Canonical Allele Identifier: CA1469474398

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179673G= , CM000666.2:g.76179673G=	GRCh38
NC_000004.11:g.77100826G= , CM000666.1:g.77100826G=	GRCh37
NC_000004.10:g.77319850G=	NCBI36
NG_012054.1:g.39210C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.432C=
ENST00000264896.8:c.456C= MANE Select	ENSP00000264896.2:p.Leu152=
ENST00000502908.2:n.1957C=
ENST00000638295.1:c.-19C=	ENSP00000492288.1:n.-19C=
ENST00000638372.1:n.708C=
ENST00000638603.1:c.456C=	ENSP00000491728.1:p.Leu152=
ENST00000638663.1:c.456C=	ENSP00000491407.1:p.Leu152=
ENST00000638680.1:n.2037C=
ENST00000639145.1:c.447C=	ENSP00000492831.1:p.Leu149=
ENST00000639300.1:c.456C=	ENSP00000492840.1:p.Leu152=
ENST00000639324.1:n.555C=
ENST00000639715.1:c.411C=
ENST00000639738.1:c.276-13372C=	ENSP00000491792.1:n.276-13372C=
ENST00000640076.1:n.37C=
ENST00000640341.1:c.*96C=	ENSP00000492714.1:n.*96C=
ENST00000640634.1:c.577C=
ENST00000640640.1:c.456C=	ENSP00000492246.1:p.Leu152=
ENST00000640916.1:n.384C=
ENST00000640957.1:c.456C=	ENSP00000492004.1:p.Leu152=
ENST00000264896.6:c.456C=	ENSP00000264896.2:p.Leu152=
ENST00000452464.6:c.276-3763C=	ENSP00000399154.2:n.276-3763C=
NM_001204255.1:c.276-3763C=	NP_001191184.1:n.276-3763C=
NM_005506.3:c.456C=	NP_005497.1:p.Leu152=
NM_005506.4:c.456C= MANE Select	NP_005497.1:p.Leu152=
NM_001204255.2:c.276-3763C=	NP_001191184.1:n.276-3763C=