Canonical Allele Identifier: CA404093985
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120517T>C , CM000681.2:g.11120517T>C GRCh38
NC_000019.9:g.11231193T>C , CM000681.1:g.11231193T>C GRCh37
NC_000019.8:g.11092193T>C NCBI36
NG_009060.1:g.36137T>C , LRG_274:g.36137T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2393T>C ENSP00000252444.6:p.Leu798Pro
ENST00000559340.2:c.*204T>C ENSP00000453696.2:n.*204T>C
ENST00000560467.2:c.2015T>C ENSP00000453513.2:p.Leu672Pro
ENST00000558518.6:c.2135T>C MANE Select ENSP00000454071.1:p.Leu712Pro
ENST00000252444.9:c.2389T>C
ENST00000455727.6:c.1631T>C ENSP00000397829.2:p.Leu544Pro
ENST00000535915.5:c.2012T>C ENSP00000440520.1:p.Leu671Pro
ENST00000545707.5:c.1606+284T>C ENSP00000437639.1:n.1606+284T>C
ENST00000557933.5:c.2135T>C ENSP00000453557.1:p.Leu712Pro
ENST00000558013.5:c.2135T>C ENSP00000453346.1:p.Leu712Pro
ENST00000558518.5:c.2135T>C ENSP00000454071.1:p.Leu712Pro
NM_000527.4:c.2135T>C , LRG_274t1:c.2135T>C NP_000518.1:p.Leu712Pro
NM_001195798.1:c.2135T>C NP_001182727.1:p.Leu712Pro
NM_001195799.1:c.2012T>C NP_001182728.1:p.Leu671Pro
NM_001195800.1:c.1631T>C NP_001182729.1:p.Leu544Pro
NM_001195803.1:c.1606+284T>C NP_001182732.1:n.1606+284T>C
XM_011528010.1:c.2135T>C XP_011526312.1:p.Leu712Pro
XM_011528011.1:c.1754T>C XP_011526313.1:p.Leu585Pro
XR_244074.2:n.2145T>C
XM_011528010.2:c.2135T>C XP_011526312.1:p.Leu712Pro
XR_001753685.2:n.2252T>C
XR_001753686.2:n.2112T>C
NM_000527.5:c.2135T>C MANE Select NP_000518.1:p.Leu712Pro
NM_001195798.2:c.2135T>C NP_001182727.1:p.Leu712Pro
NM_001195799.2:c.2012T>C NP_001182728.1:p.Leu671Pro
NM_001195800.2:c.1631T>C NP_001182729.1:p.Leu544Pro
NM_001195803.2:c.1606+284T>C NP_001182732.1:n.1606+284T>C