Canonical Allele Identifier: CA029390

Gene: LDLR

Linked Data

• dbSNP Id: rs780093891
• ExAC: 19:11217337 T / C
• gnomAD v2: 19-11217337-T-C
• gnomAD v4: 19-11106661-T-C
• MyVariant Identifiers: chr19:g.11217337T>C (hg19) ; chr19:g.11106661T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11106661T>C , CM000681.2:g.11106661T>C	GRCh38
NC_000019.9:g.11217337T>C , CM000681.1:g.11217337T>C	GRCh37
NC_000019.8:g.11078337T>C	NCBI36
NG_009060.1:g.22281T>C , LRG_274:g.22281T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1049T>C	ENSP00000252444.6:p.Met350Thr
ENST00000559340.2:c.791T>C	ENSP00000453696.2:p.Met264Thr
ENST00000560467.2:c.791T>C	ENSP00000453513.2:p.Met264Thr
ENST00000558518.6:c.791T>C MANE Select	ENSP00000454071.1:p.Met264Thr
ENST00000252444.9:c.1045T>C
ENST00000455727.6:c.314-731T>C	ENSP00000397829.2:n.314-731T>C
ENST00000535915.5:c.668T>C	ENSP00000440520.1:p.Met223Thr
ENST00000545707.5:c.410T>C	ENSP00000437639.1:p.Met137Thr
ENST00000557933.5:c.791T>C	ENSP00000453557.1:p.Met264Thr
ENST00000558013.5:c.791T>C	ENSP00000453346.1:p.Met264Thr
ENST00000558518.5:c.791T>C	ENSP00000454071.1:p.Met264Thr
ENST00000558528.1:n.306T>C
ENST00000560467.1:c.391T>C
NM_000527.4:c.791T>C , LRG_274t1:c.791T>C	NP_000518.1:p.Met264Thr
NM_001195798.1:c.791T>C	NP_001182727.1:p.Met264Thr
NM_001195799.1:c.668T>C	NP_001182728.1:p.Met223Thr
NM_001195800.1:c.314-731T>C	NP_001182729.1:n.314-731T>C
NM_001195803.1:c.410T>C	NP_001182732.1:p.Met137Thr
XM_011528010.1:c.791T>C	XP_011526312.1:p.Met264Thr
XM_011528011.1:c.410T>C	XP_011526313.1:p.Met137Thr
XR_244074.2:n.941T>C
XM_011528010.2:c.791T>C	XP_011526312.1:p.Met264Thr
XR_001753685.2:n.908T>C
XR_001753686.2:n.908T>C
NM_000527.5:c.791T>C MANE Select	NP_000518.1:p.Met264Thr
NM_001195798.2:c.791T>C	NP_001182727.1:p.Met264Thr
NM_001195799.2:c.668T>C	NP_001182728.1:p.Met223Thr
NM_001195800.2:c.314-731T>C	NP_001182729.1:n.314-731T>C
NM_001195803.2:c.410T>C	NP_001182732.1:p.Met137Thr