Canonical Allele Identifier: CA404099786

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11240326G>C (hg19) ; chr19:g.11129650G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11129650G>C , CM000681.2:g.11129650G>C	GRCh38
NC_000019.9:g.11240326G>C , CM000681.1:g.11240326G>C	GRCh37
NC_000019.8:g.11101326G>C	NCBI36
NG_009060.1:g.45270G>C , LRG_274:g.45270G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2785G>C	ENSP00000252444.6:p.Asp929His
ENST00000559340.2:c.*596G>C	ENSP00000453696.2:n.*596G>C
ENST00000560467.2:c.2407G>C	ENSP00000453513.2:p.Asp803His
ENST00000558518.6:c.2527G>C MANE Select	ENSP00000454071.1:p.Asp843His
ENST00000252444.9:c.2781G>C
ENST00000455727.6:c.2023G>C	ENSP00000397829.2:p.Asp675His
ENST00000535915.5:c.2404G>C	ENSP00000440520.1:p.Asp802His
ENST00000545707.5:c.1993G>C	ENSP00000437639.1:p.Asp665His
ENST00000557933.5:c.2589G>C	ENSP00000453557.1:p.Arg863Ser
ENST00000558013.5:c.2527G>C	ENSP00000453346.1:p.Asp843His
ENST00000558518.5:c.2527G>C	ENSP00000454071.1:p.Asp843His
ENST00000560628.1:n.108+1996G>C
NM_000527.4:c.2527G>C , LRG_274t1:c.2527G>C	NP_000518.1:p.Asp843His
NM_001195798.1:c.2527G>C	NP_001182727.1:p.Asp843His
NM_001195799.1:c.2404G>C	NP_001182728.1:p.Asp802His
NM_001195800.1:c.2023G>C	NP_001182729.1:p.Asp675His
NM_001195803.1:c.1993G>C	NP_001182732.1:p.Asp665His
XM_011528010.1:c.2449G>C	XP_011526312.1:p.Asp817His
XM_011528011.1:c.2146G>C	XP_011526313.1:p.Asp716His
XM_011528010.2:c.2449G>C	XP_011526312.1:p.Asp817His
XR_001753685.2:n.2861G>C
XR_001753686.2:n.2504G>C
NM_000527.5:c.2527G>C MANE Select	NP_000518.1:p.Asp843His
NM_001195798.2:c.2527G>C	NP_001182727.1:p.Asp843His
NM_001195799.2:c.2404G>C	NP_001182728.1:p.Asp802His
NM_001195800.2:c.2023G>C	NP_001182729.1:p.Asp675His
NM_001195803.2:c.1993G>C	NP_001182732.1:p.Asp665His