Canonical Allele Identifier: CA2069525204

Gene: SCARB1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124863717C= , CM000674.2:g.124863717C=	GRCh38
NC_000012.11:g.125348263C= , CM000674.1:g.125348263C=	GRCh37
NC_000012.10:g.123914216C=	NCBI36
NG_028199.1:g.5257G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005505.5:c.4G= MANE Select	NP_005496.4:p.Gly2=
ENST00000261693.11:c.4G= MANE Select	ENSP00000261693.6:p.Gly2=
NM_001082959.1:c.4G=	NP_001076428.1:p.Gly2=
NM_001082959.2:c.4G=	NP_001076428.1:p.Gly2=
NM_001367981.1:c.4G=	NP_001354910.1:p.Gly2=
NM_001367983.1:c.4G=	NP_001354912.1:p.Gly2=
NM_001367984.1:c.4G=	NP_001354913.1:p.Gly2=
NM_001367985.1:c.4G=	NP_001354914.1:p.Gly2=
NM_001367986.1:c.4G=	NP_001354915.1:p.Gly2=
NM_001367987.1:c.4G=	NP_001354916.1:p.Gly2=
NM_001367988.1:c.4G=	NP_001354917.1:p.Gly2=
NM_001367989.1:c.4G=	NP_001354918.1:p.Gly2=
NM_005505.4:c.4G=	NP_005496.4:p.Gly2=
NR_160416.1:n.148G=
NR_160417.1:n.148G=
NR_160418.1:n.148G=
NR_160419.1:n.148G=
NR_160420.1:n.148G=
NR_160421.1:n.148G=
NR_160422.1:n.148G=
NR_160423.1:n.148G=
NR_160424.1:n.148G=
ENST00000261693.10:c.4G=	ENSP00000261693.6:p.Gly2=
ENST00000339570.9:c.4G=	ENSP00000343795.4:p.Gly2=
ENST00000415380.6:c.4G=	ENSP00000414979.2:p.Gly2=
ENST00000535005.5:n.441+3272G=
ENST00000538291.5:n.147G=
ENST00000539320.2:n.180G=
ENST00000539320.3:n.237G=
ENST00000541661.5:n.167+18785G=
ENST00000545493.1:c.4G=	ENSP00000443454.1:p.Gly2=
ENST00000546215.5:c.4G=	ENSP00000442862.1:p.Gly2=
ENST00000679605.1:c.4G=	ENSP00000505370.1:p.Gly2=
ENST00000680556.1:c.4G=	ENSP00000505757.1:p.Gly2=
ENST00000680596.1:c.4G=	ENSP00000505605.1:p.Gly2=
ENST00000680926.1:c.4G=	ENSP00000505571.1:p.Gly2=
ENST00000680982.1:c.4G=	ENSP00000506281.1:p.Gly2=
ENST00000681117.1:c.4G=	ENSP00000506693.1:p.Gly2=
ENST00000681686.1:c.4G=	ENSP00000505406.1:p.Gly2=