Canonical Allele Identifier: CA2322768637

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107486C= , CM000681.2:g.11107486C=	GRCh38
NC_000019.9:g.11218162C= , CM000681.1:g.11218162C=	GRCh37
NC_000019.8:g.11079162C=	NCBI36
NG_009060.1:g.23106C= , LRG_274:g.23106C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1170C=	ENSP00000252444.6:p.Asp390=
ENST00000559340.2:c.912C=	ENSP00000453696.2:p.Asp304=
ENST00000560467.2:c.912C=	ENSP00000453513.2:p.Asp304=
ENST00000558518.6:c.912C= MANE Select	ENSP00000454071.1:p.Asp304=
ENST00000252444.9:c.1166C=
ENST00000455727.6:c.408C=	ENSP00000397829.2:p.Asp136=
ENST00000535915.5:c.789C=	ENSP00000440520.1:p.Asp263=
ENST00000545707.5:c.531C=	ENSP00000437639.1:p.Asp177=
ENST00000557933.5:c.912C=	ENSP00000453557.1:p.Asp304=
ENST00000558013.5:c.912C=	ENSP00000453346.1:p.Asp304=
ENST00000558518.5:c.912C=	ENSP00000454071.1:p.Asp304=
ENST00000558528.1:n.427C=
ENST00000560467.1:c.512C=
NM_000527.4:c.912C= , LRG_274t1:c.912C=	NP_000518.1:p.Asp304=
NM_001195798.1:c.912C=	NP_001182727.1:p.Asp304=
NM_001195799.1:c.789C=	NP_001182728.1:p.Asp263=
NM_001195800.1:c.408C=	NP_001182729.1:p.Asp136=
NM_001195803.1:c.531C=	NP_001182732.1:p.Asp177=
XM_011528010.1:c.912C=	XP_011526312.1:p.Asp304=
XM_011528011.1:c.531C=	XP_011526313.1:p.Asp177=
XR_244074.2:n.1062C=
XM_011528010.2:c.912C=	XP_011526312.1:p.Asp304=
XR_001753685.2:n.1029C=
XR_001753686.2:n.1029C=
NM_000527.5:c.912C= MANE Select	NP_000518.1:p.Asp304=
NM_001195798.2:c.912C=	NP_001182727.1:p.Asp304=
NM_001195799.2:c.789C=	NP_001182728.1:p.Asp263=
NM_001195800.2:c.408C=	NP_001182729.1:p.Asp136=
NM_001195803.2:c.531C=	NP_001182732.1:p.Asp177=