Canonical Allele Identifier: CA2830556204
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120721_11120722insCAGGGGGCCGGGAAAGAGGAA , CM000681.2:g.11120721_11120722insCAGGGGGCCGGGAAAGAGGAA GRCh38
NC_000019.9:g.11231397_11231398insCAGGGGGCCGGGAAAGAGGAA , CM000681.1:g.11231397_11231398insCAGGGGGCCGGGAAAGAGGAA GRCh37
NC_000019.8:g.11092397_11092398insCAGGGGGCCGGGAAAGAGGAA NCBI36
NG_009060.1:g.36341_36342insCAGGGGGCCGGGAAAGAGGAA , LRG_274:g.36341_36342insCAGGGGGCCGGGAAAGAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2398+199_2398+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000252444.6:n.2398+199_2398+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000559340.2:c.*209+199_*209+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000453696.2:n.*209+199_*209+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000560467.2:c.2020+199_2020+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000453513.2:n.2020+199_2020+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000558518.6:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA MANE Select ENSP00000454071.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000252444.9:c.2394+199_2394+200insCAGGGGGCCGGGAAAGAGGAA
ENST00000455727.6:c.1636+199_1636+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000397829.2:n.1636+199_1636+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000535915.5:c.2017+199_2017+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000440520.1:n.2017+199_2017+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000545707.5:c.1606+488_1606+489insCAGGGGGCCGGGAAAGAGGAA ENSP00000437639.1:n.1606+488_1606+489insCAGGGGGCCGGGAAAGAGGAA...
ENST00000557933.5:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000453557.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000558013.5:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000453346.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA...
ENST00000558518.5:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA ENSP00000454071.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA...
NM_000527.4:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA , LRG_274t1:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA NP_000518.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195798.1:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA NP_001182727.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195799.1:c.2017+199_2017+200insCAGGGGGCCGGGAAAGAGGAA NP_001182728.1:n.2017+199_2017+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195800.1:c.1636+199_1636+200insCAGGGGGCCGGGAAAGAGGAA NP_001182729.1:n.1636+199_1636+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195803.1:c.1606+488_1606+489insCAGGGGGCCGGGAAAGAGGAA NP_001182732.1:n.1606+488_1606+489insCAGGGGGCCGGGAAAGAGGAA
XM_011528010.1:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA XP_011526312.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA
XM_011528011.1:c.1759+199_1759+200insCAGGGGGCCGGGAAAGAGGAA XP_011526313.1:n.1759+199_1759+200insCAGGGGGCCGGGAAAGAGGAA
XR_244074.2:n.2150+199_2150+200insCAGGGGGCCGGGAAAGAGGAA
XM_011528010.2:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA XP_011526312.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA
XR_001753685.2:n.2456_2457insCAGGGGGCCGGGAAAGAGGAA
XR_001753686.2:n.2117+199_2117+200insCAGGGGGCCGGGAAAGAGGAA
NM_000527.5:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA MANE Select NP_000518.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195798.2:c.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA NP_001182727.1:n.2140+199_2140+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195799.2:c.2017+199_2017+200insCAGGGGGCCGGGAAAGAGGAA NP_001182728.1:n.2017+199_2017+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195800.2:c.1636+199_1636+200insCAGGGGGCCGGGAAAGAGGAA NP_001182729.1:n.1636+199_1636+200insCAGGGGGCCGGGAAAGAGGAA
NM_001195803.2:c.1606+488_1606+489insCAGGGGGCCGGGAAAGAGGAA NP_001182732.1:n.1606+488_1606+489insCAGGGGGCCGGGAAAGAGGAA