Canonical Allele Identifier: CA404080605

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11218093G>C (hg19) ; chr19:g.11107417G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107417G>C , CM000681.2:g.11107417G>C	GRCh38
NC_000019.9:g.11218093G>C , CM000681.1:g.11218093G>C	GRCh37
NC_000019.8:g.11079093G>C	NCBI36
NG_009060.1:g.23037G>C , LRG_274:g.23037G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1101G>C	ENSP00000252444.6:p.Lys367Asn
ENST00000559340.2:c.843G>C	ENSP00000453696.2:p.Lys281Asn
ENST00000560467.2:c.843G>C	ENSP00000453513.2:p.Lys281Asn
ENST00000558518.6:c.843G>C MANE Select	ENSP00000454071.1:p.Lys281Asn
ENST00000252444.9:c.1097G>C
ENST00000455727.6:c.339G>C	ENSP00000397829.2:p.Lys113Asn
ENST00000535915.5:c.720G>C	ENSP00000440520.1:p.Lys240Asn
ENST00000545707.5:c.462G>C	ENSP00000437639.1:p.Lys154Asn
ENST00000557933.5:c.843G>C	ENSP00000453557.1:p.Lys281Asn
ENST00000558013.5:c.843G>C	ENSP00000453346.1:p.Lys281Asn
ENST00000558518.5:c.843G>C	ENSP00000454071.1:p.Lys281Asn
ENST00000558528.1:n.358G>C
ENST00000560467.1:c.443G>C
NM_000527.4:c.843G>C , LRG_274t1:c.843G>C	NP_000518.1:p.Lys281Asn
NM_001195798.1:c.843G>C	NP_001182727.1:p.Lys281Asn
NM_001195799.1:c.720G>C	NP_001182728.1:p.Lys240Asn
NM_001195800.1:c.339G>C	NP_001182729.1:p.Lys113Asn
NM_001195803.1:c.462G>C	NP_001182732.1:p.Lys154Asn
XM_011528010.1:c.843G>C	XP_011526312.1:p.Lys281Asn
XM_011528011.1:c.462G>C	XP_011526313.1:p.Lys154Asn
XR_244074.2:n.993G>C
XM_011528010.2:c.843G>C	XP_011526312.1:p.Lys281Asn
XR_001753685.2:n.960G>C
XR_001753686.2:n.960G>C
NM_000527.5:c.843G>C MANE Select	NP_000518.1:p.Lys281Asn
NM_001195798.2:c.843G>C	NP_001182727.1:p.Lys281Asn
NM_001195799.2:c.720G>C	NP_001182728.1:p.Lys240Asn
NM_001195800.2:c.339G>C	NP_001182729.1:p.Lys113Asn
NM_001195803.2:c.462G>C	NP_001182732.1:p.Lys154Asn