Canonical Allele Identifier: CA2322779554

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11128070A= , CM000681.2:g.11128070A=	GRCh38
NC_000019.9:g.11238746A= , CM000681.1:g.11238746A=	GRCh37
NC_000019.8:g.11099746A=	NCBI36
NG_009060.1:g.43690A= , LRG_274:g.43690A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2632A=	ENSP00000252444.6:p.Ile878=
ENST00000559340.2:c.*443A=	ENSP00000453696.2:n.*443A=
ENST00000560467.2:c.2254A=	ENSP00000453513.2:p.Ile752=
ENST00000558518.6:c.2374A= MANE Select	ENSP00000454071.1:p.Ile792=
ENST00000252444.9:c.2628A=
ENST00000455727.6:c.1870A=	ENSP00000397829.2:p.Ile624=
ENST00000535915.5:c.2251A=	ENSP00000440520.1:p.Ile751=
ENST00000545707.5:c.1840A=	ENSP00000437639.1:p.Ile614=
ENST00000557933.5:c.2374A=	ENSP00000453557.1:p.Ile792=
ENST00000558013.5:c.2374A=	ENSP00000453346.1:p.Ile792=
ENST00000558518.5:c.2374A=	ENSP00000454071.1:p.Ile792=
ENST00000560628.1:n.108+416A=
NM_000527.4:c.2374A= , LRG_274t1:c.2374A=	NP_000518.1:p.Ile792=
NM_001195798.1:c.2374A=	NP_001182727.1:p.Ile792=
NM_001195799.1:c.2251A=	NP_001182728.1:p.Ile751=
NM_001195800.1:c.1870A=	NP_001182729.1:p.Ile624=
NM_001195803.1:c.1840A=	NP_001182732.1:p.Ile614=
XM_011528010.1:c.2312-1443A=	XP_011526312.1:n.2312-1443A=
XM_011528011.1:c.1993A=	XP_011526313.1:p.Ile665=
XR_244074.2:n.2384A=
XM_011528010.2:c.2312-1443A=	XP_011526312.1:n.2312-1443A=
XR_001753685.2:n.2708A=
XR_001753686.2:n.2351A=
NM_000527.5:c.2374A= MANE Select	NP_000518.1:p.Ile792=
NM_001195798.2:c.2374A=	NP_001182727.1:p.Ile792=
NM_001195799.2:c.2251A=	NP_001182728.1:p.Ile751=
NM_001195800.2:c.1870A=	NP_001182729.1:p.Ile624=
NM_001195803.2:c.1840A=	NP_001182732.1:p.Ile614=