Canonical Allele Identifier: CA2735613943
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs2147283820

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128143_11128144insG , CM000681.2:g.11128143_11128144insG GRCh38
NC_000019.9:g.11238819_11238820insG , CM000681.1:g.11238819_11238820insG GRCh37
NC_000019.8:g.11099819_11099820insG NCBI36
NG_009060.1:g.43763_43764insG , LRG_274:g.43763_43764insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2647+58_2647+59insG ENSP00000252444.6:n.2647+58_2647+59insG
ENST00000559340.2:c.*458+58_*458+59insG ENSP00000453696.2:n.*458+58_*458+59insG
ENST00000560467.2:c.2269+58_2269+59insG ENSP00000453513.2:n.2269+58_2269+59insG
ENST00000558518.6:c.2389+58_2389+59insG MANE Select ENSP00000454071.1:n.2389+58_2389+59insG
ENST00000252444.9:c.2643+58_2643+59insG
ENST00000455727.6:c.1885+58_1885+59insG ENSP00000397829.2:n.1885+58_1885+59insG
ENST00000535915.5:c.2266+58_2266+59insG ENSP00000440520.1:n.2266+58_2266+59insG
ENST00000545707.5:c.1855+58_1855+59insG ENSP00000437639.1:n.1855+58_1855+59insG
ENST00000557933.5:c.2389+58_2389+59insG ENSP00000453557.1:n.2389+58_2389+59insG
ENST00000558013.5:c.2389+58_2389+59insG ENSP00000453346.1:n.2389+58_2389+59insG
ENST00000558518.5:c.2389+58_2389+59insG ENSP00000454071.1:n.2389+58_2389+59insG
ENST00000560628.1:n.108+489_108+490insG
NM_000527.4:c.2389+58_2389+59insG , LRG_274t1:c.2389+58_2389+59insG NP_000518.1:n.2389+58_2389+59insG
NM_001195798.1:c.2389+58_2389+59insG NP_001182727.1:n.2389+58_2389+59insG
NM_001195799.1:c.2266+58_2266+59insG NP_001182728.1:n.2266+58_2266+59insG
NM_001195800.1:c.1885+58_1885+59insG NP_001182729.1:n.1885+58_1885+59insG
NM_001195803.1:c.1855+58_1855+59insG NP_001182732.1:n.1855+58_1855+59insG
XM_011528010.1:c.2312-1370_2312-1369insG XP_011526312.1:n.2312-1370_2312-1369insG
XM_011528011.1:c.2008+58_2008+59insG XP_011526313.1:n.2008+58_2008+59insG
XR_244074.2:n.2399+58_2399+59insG
XM_011528010.2:c.2312-1370_2312-1369insG XP_011526312.1:n.2312-1370_2312-1369insG
XR_001753685.2:n.2723+58_2723+59insG
XR_001753686.2:n.2366+58_2366+59insG
NM_000527.5:c.2389+58_2389+59insG MANE Select NP_000518.1:n.2389+58_2389+59insG
NM_001195798.2:c.2389+58_2389+59insG NP_001182727.1:n.2389+58_2389+59insG
NM_001195799.2:c.2266+58_2266+59insG NP_001182728.1:n.2266+58_2266+59insG
NM_001195800.2:c.1885+58_1885+59insG NP_001182729.1:n.1885+58_1885+59insG
NM_001195803.2:c.1855+58_1855+59insG NP_001182732.1:n.1855+58_1855+59insG