Canonical Allele Identifier: CA2322767385

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11105346C= , CM000681.2:g.11105346C=	GRCh38
NC_000019.9:g.11216022C= , CM000681.1:g.11216022C=	GRCh37
NC_000019.8:g.11077022C=	NCBI36
NG_009060.1:g.20966C= , LRG_274:g.20966C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.698C=	ENSP00000252444.6:p.Thr233=
ENST00000559340.2:c.440C=	ENSP00000453696.2:p.Thr147=
ENST00000560467.2:c.440C=	ENSP00000453513.2:p.Thr147=
ENST00000558518.6:c.440C= MANE Select	ENSP00000454071.1:p.Thr147=
ENST00000252444.9:c.694C=
ENST00000455727.6:c.314-2046C=	ENSP00000397829.2:n.314-2046C=
ENST00000535915.5:c.317C=	ENSP00000440520.1:p.Thr106=
ENST00000545707.5:c.314-1219C=	ENSP00000437639.1:n.314-1219C=
ENST00000557933.5:c.440C=	ENSP00000453557.1:p.Thr147=
ENST00000558013.5:c.440C=	ENSP00000453346.1:p.Thr147=
ENST00000558518.5:c.440C=	ENSP00000454071.1:p.Thr147=
ENST00000560467.1:c.40C=
NM_000527.4:c.440C= , LRG_274t1:c.440C=	NP_000518.1:p.Thr147=
NM_001195798.1:c.440C=	NP_001182727.1:p.Thr147=
NM_001195799.1:c.317C=	NP_001182728.1:p.Thr106=
NM_001195800.1:c.314-2046C=	NP_001182729.1:n.314-2046C=
NM_001195803.1:c.314-1219C=	NP_001182732.1:n.314-1219C=
XM_011528010.1:c.440C=	XP_011526312.1:p.Thr147=
XM_011528011.1:c.314-1219C=	XP_011526313.1:n.314-1219C=
XR_244074.2:n.590C=
XM_011528010.2:c.440C=	XP_011526312.1:p.Thr147=
XR_001753685.2:n.557C=
XR_001753686.2:n.557C=
NM_000527.5:c.440C= MANE Select	NP_000518.1:p.Thr147=
NM_001195798.2:c.440C=	NP_001182727.1:p.Thr147=
NM_001195799.2:c.317C=	NP_001182728.1:p.Thr106=
NM_001195800.2:c.314-2046C=	NP_001182729.1:n.314-2046C=
NM_001195803.2:c.314-1219C=	NP_001182732.1:n.314-1219C=