Canonical Allele Identifier: CA1469474012

Gene: SCARB2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76179523G= , CM000666.2:g.76179523G=	GRCh38
NC_000004.11:g.77100676G= , CM000666.1:g.77100676G=	GRCh37
NC_000004.10:g.77319700G=	NCBI36
NG_012054.1:g.39360C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682785.1:n.582C=
ENST00000264896.8:c.606C= MANE Select	ENSP00000264896.2:p.Phe202=
ENST00000502908.2:n.2107C=
ENST00000638295.1:c.132C=	ENSP00000492288.1:p.Phe44=
ENST00000638372.1:n.858C=
ENST00000638603.1:c.606C=	ENSP00000491728.1:p.Phe202=
ENST00000638663.1:c.606C=	ENSP00000491407.1:p.Phe202=
ENST00000638680.1:n.2187C=
ENST00000639145.1:c.597C=	ENSP00000492831.1:p.Phe199=
ENST00000639300.1:c.606C=	ENSP00000492840.1:p.Phe202=
ENST00000639324.1:n.705C=
ENST00000639715.1:c.561C=
ENST00000639738.1:c.276-13222C=	ENSP00000491792.1:n.276-13222C=
ENST00000640076.1:n.187C=
ENST00000640341.1:c.*246C=	ENSP00000492714.1:n.*246C=
ENST00000640634.1:c.727C=
ENST00000640640.1:c.606C=	ENSP00000492246.1:p.Phe202=
ENST00000640916.1:n.534C=
ENST00000640957.1:c.606C=	ENSP00000492004.1:p.Phe202=
ENST00000264896.6:c.606C=	ENSP00000264896.2:p.Phe202=
ENST00000452464.6:c.276-3613C=	ENSP00000399154.2:n.276-3613C=
NM_001204255.1:c.276-3613C=	NP_001191184.1:n.276-3613C=
NM_005506.3:c.606C=	NP_005497.1:p.Phe202=
NM_005506.4:c.606C= MANE Select	NP_005497.1:p.Phe202=
NM_001204255.2:c.276-3613C=	NP_001191184.1:n.276-3613C=