Canonical Allele Identifier: CA10584802
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251087
ClinVar RCV Id: RCV000237930
dbSNP Id: rs879254444

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11102713C>A , CM000681.2:g.11102713C>A GRCh38
NC_000019.9:g.11213389C>A , CM000681.1:g.11213389C>A GRCh37
NC_000019.8:g.11074389C>A NCBI36
NG_009060.1:g.18333C>A , LRG_274:g.18333C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.498C>A ENSP00000252444.6:p.Asn166Lys
ENST00000559340.2:c.240C>A ENSP00000453696.2:p.Asn80Lys
ENST00000560467.2:c.240C>A ENSP00000453513.2:p.Asn80Lys
ENST00000558518.6:c.240C>A MANE Select ENSP00000454071.1:p.Asn80Lys
ENST00000252444.9:c.494C>A
ENST00000455727.6:c.240C>A ENSP00000397829.2:p.Asn80Lys
ENST00000535915.5:c.190+2368C>A ENSP00000440520.1:n.190+2368C>A
ENST00000545707.5:c.240C>A ENSP00000437639.1:p.Asn80Lys
ENST00000557933.5:c.240C>A ENSP00000453557.1:p.Asn80Lys
ENST00000557958.1:n.326C>A
ENST00000558013.5:c.240C>A ENSP00000453346.1:p.Asn80Lys
ENST00000558518.5:c.240C>A ENSP00000454071.1:p.Asn80Lys
NM_000527.4:c.240C>A , LRG_274t1:c.240C>A NP_000518.1:p.Asn80Lys
NM_001195798.1:c.240C>A NP_001182727.1:p.Asn80Lys
NM_001195799.1:c.190+2368C>A NP_001182728.1:n.190+2368C>A
NM_001195800.1:c.240C>A NP_001182729.1:p.Asn80Lys
NM_001195803.1:c.240C>A NP_001182732.1:p.Asn80Lys
XM_011528010.1:c.240C>A XP_011526312.1:p.Asn80Lys
XM_011528011.1:c.240C>A XP_011526313.1:p.Asn80Lys
XR_244074.2:n.390C>A
XM_011528010.2:c.240C>A XP_011526312.1:p.Asn80Lys
XR_001753685.2:n.357C>A
XR_001753686.2:n.357C>A
NM_000527.5:c.240C>A MANE Select NP_000518.1:p.Asn80Lys
NM_001195798.2:c.240C>A NP_001182727.1:p.Asn80Lys
NM_001195799.2:c.190+2368C>A NP_001182728.1:n.190+2368C>A
NM_001195800.2:c.240C>A NP_001182729.1:p.Asn80Lys
NM_001195803.2:c.240C>A NP_001182732.1:p.Asn80Lys