Canonical Allele Identifier: CA041649
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 922750
dbSNP Id: rs562712652

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11100228G>A , CM000681.2:g.11100228G>A GRCh38
NC_000019.9:g.11210904G>A , CM000681.1:g.11210904G>A GRCh37
NC_000019.8:g.11071904G>A NCBI36
NG_009060.1:g.15848G>A , LRG_274:g.15848G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.331G>A ENSP00000252444.6:p.Asp111Asn
ENST00000559340.2:c.73G>A ENSP00000453696.2:p.Asp25Asn
ENST00000560467.2:c.73G>A ENSP00000453513.2:p.Asp25Asn
ENST00000558518.6:c.73G>A MANE Select ENSP00000454071.1:p.Asp25Asn
ENST00000252444.9:c.327G>A
ENST00000455727.6:c.73G>A ENSP00000397829.2:p.Asp25Asn
ENST00000535915.5:c.73G>A ENSP00000440520.1:p.Asp25Asn
ENST00000545707.5:c.73G>A ENSP00000437639.1:p.Asp25Asn
ENST00000557933.5:c.73G>A ENSP00000453557.1:p.Asp25Asn
ENST00000557958.1:n.159G>A
ENST00000558013.5:c.73G>A ENSP00000453346.1:p.Asp25Asn
ENST00000558518.5:c.73G>A ENSP00000454071.1:p.Asp25Asn
ENST00000560502.5:n.159G>A
NM_000527.4:c.73G>A , LRG_274t1:c.73G>A NP_000518.1:p.Asp25Asn
NM_001195798.1:c.73G>A NP_001182727.1:p.Asp25Asn
NM_001195799.1:c.73G>A NP_001182728.1:p.Asp25Asn
NM_001195800.1:c.73G>A NP_001182729.1:p.Asp25Asn
NM_001195803.1:c.73G>A NP_001182732.1:p.Asp25Asn
XM_011528010.1:c.73G>A XP_011526312.1:p.Asp25Asn
XM_011528011.1:c.73G>A XP_011526313.1:p.Asp25Asn
XR_244074.2:n.223G>A
XM_011528010.2:c.73G>A XP_011526312.1:p.Asp25Asn
XR_001753685.2:n.190G>A
XR_001753686.2:n.190G>A
NM_000527.5:c.73G>A MANE Select NP_000518.1:p.Asp25Asn
NM_001195798.2:c.73G>A NP_001182727.1:p.Asp25Asn
NM_001195799.2:c.73G>A NP_001182728.1:p.Asp25Asn
NM_001195800.2:c.73G>A NP_001182729.1:p.Asp25Asn
NM_001195803.2:c.73G>A NP_001182732.1:p.Asp25Asn