Canonical Allele Identifier: CA404094772

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11233859C>T (hg19) ; chr19:g.11123183C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11123183C>T , CM000681.2:g.11123183C>T	GRCh38
NC_000019.9:g.11233859C>T , CM000681.1:g.11233859C>T	GRCh37
NC_000019.8:g.11094859C>T	NCBI36
NG_009060.1:g.38803C>T , LRG_274:g.38803C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2408C>T	ENSP00000252444.6:p.Ala803Val
ENST00000559340.2:c.*219C>T	ENSP00000453696.2:n.*219C>T
ENST00000560467.2:c.2030C>T	ENSP00000453513.2:p.Ala677Val
ENST00000558518.6:c.2150C>T MANE Select	ENSP00000454071.1:p.Ala717Val
ENST00000252444.9:c.2404C>T
ENST00000455727.6:c.1646C>T	ENSP00000397829.2:p.Ala549Val
ENST00000535915.5:c.2027C>T	ENSP00000440520.1:p.Ala676Val
ENST00000545707.5:c.1616C>T	ENSP00000437639.1:p.Ala539Val
ENST00000557933.5:c.2150C>T	ENSP00000453557.1:p.Ala717Val
ENST00000558013.5:c.2150C>T	ENSP00000453346.1:p.Ala717Val
ENST00000558518.5:c.2150C>T	ENSP00000454071.1:p.Ala717Val
NM_000527.4:c.2150C>T , LRG_274t1:c.2150C>T	NP_000518.1:p.Ala717Val
NM_001195798.1:c.2150C>T	NP_001182727.1:p.Ala717Val
NM_001195799.1:c.2027C>T	NP_001182728.1:p.Ala676Val
NM_001195800.1:c.1646C>T	NP_001182729.1:p.Ala549Val
NM_001195803.1:c.1616C>T	NP_001182732.1:p.Ala539Val
XM_011528010.1:c.2150C>T	XP_011526312.1:p.Ala717Val
XM_011528011.1:c.1769C>T	XP_011526313.1:p.Ala590Val
XR_244074.2:n.2160C>T
XM_011528010.2:c.2150C>T	XP_011526312.1:p.Ala717Val
XR_001753685.2:n.2484C>T
XR_001753686.2:n.2127C>T
NM_000527.5:c.2150C>T MANE Select	NP_000518.1:p.Ala717Val
NM_001195798.2:c.2150C>T	NP_001182727.1:p.Ala717Val
NM_001195799.2:c.2027C>T	NP_001182728.1:p.Ala676Val
NM_001195800.2:c.1646C>T	NP_001182729.1:p.Ala549Val
NM_001195803.2:c.1616C>T	NP_001182732.1:p.Ala539Val