Canonical Allele Identifier: CA631764674
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2077327717

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11108219_11108220insAAA , CM000681.2:g.11108219_11108220insAAA GRCh38
NC_000019.9:g.11218895_11218896insAAA , CM000681.1:g.11218895_11218896insAAA GRCh37
NC_000019.8:g.11079895_11079896insAAA NCBI36
NG_009060.1:g.23839_23840insAAA , LRG_274:g.23839_23840insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1198+705_1198+706insAAA ENSP00000252444.6:n.1198+705_1198+706insAAA
ENST00000559340.2:c.940+705_940+706insAAA ENSP00000453696.2:n.940+705_940+706insAAA
ENST00000560467.2:c.940+705_940+706insAAA ENSP00000453513.2:n.940+705_940+706insAAA
ENST00000558518.6:c.940+705_940+706insAAA MANE Select ENSP00000454071.1:n.940+705_940+706insAAA
ENST00000252444.9:c.1194+705_1194+706insAAA
ENST00000455727.6:c.436+705_436+706insAAA ENSP00000397829.2:n.436+705_436+706insAAA
ENST00000535915.5:c.817+705_817+706insAAA ENSP00000440520.1:n.817+705_817+706insAAA
ENST00000545707.5:c.559+705_559+706insAAA ENSP00000437639.1:n.559+705_559+706insAAA
ENST00000557933.5:c.940+705_940+706insAAA ENSP00000453557.1:n.940+705_940+706insAAA
ENST00000558013.5:c.940+705_940+706insAAA ENSP00000453346.1:n.940+705_940+706insAAA
ENST00000558518.5:c.940+705_940+706insAAA ENSP00000454071.1:n.940+705_940+706insAAA
ENST00000560467.1:c.540+705_540+706insAAA
NM_000527.4:c.940+705_940+706insAAA , LRG_274t1:c.940+705_940+706insAAA NP_000518.1:n.940+705_940+706insAAA
NM_001195798.1:c.940+705_940+706insAAA NP_001182727.1:n.940+705_940+706insAAA
NM_001195799.1:c.817+705_817+706insAAA NP_001182728.1:n.817+705_817+706insAAA
NM_001195800.1:c.436+705_436+706insAAA NP_001182729.1:n.436+705_436+706insAAA
NM_001195803.1:c.559+705_559+706insAAA NP_001182732.1:n.559+705_559+706insAAA
XM_011528010.1:c.940+705_940+706insAAA XP_011526312.1:n.940+705_940+706insAAA
XM_011528011.1:c.559+705_559+706insAAA XP_011526313.1:n.559+705_559+706insAAA
XR_244074.2:n.1090+705_1090+706insAAA
XM_011528010.2:c.940+705_940+706insAAA XP_011526312.1:n.940+705_940+706insAAA
XR_001753685.2:n.1057+705_1057+706insAAA
XR_001753686.2:n.1057+705_1057+706insAAA
NM_000527.5:c.940+705_940+706insAAA MANE Select NP_000518.1:n.940+705_940+706insAAA
NM_001195798.2:c.940+705_940+706insAAA NP_001182727.1:n.940+705_940+706insAAA
NM_001195799.2:c.817+705_817+706insAAA NP_001182728.1:n.817+705_817+706insAAA
NM_001195800.2:c.436+705_436+706insAAA NP_001182729.1:n.436+705_436+706insAAA
NM_001195803.2:c.559+705_559+706insAAA NP_001182732.1:n.559+705_559+706insAAA