Canonical Allele Identifier: CA2069464193

Gene: SCARB1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124776940T= , CM000674.2:g.124776940T=	GRCh38
NC_000012.11:g.125261486T= , CM000674.1:g.125261486T=	GRCh37
NC_000012.10:g.123827439T=	NCBI36
NG_028199.1:g.92034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1647A= MANE Select	ENSP00000261693.6:n.*1647A=
ENST00000339570.9:c.*1527A=	ENSP00000343795.4:n.*1527A=
NM_005505.5:c.*1647A= MANE Select	NP_005496.4:n.*1647A=
NM_001082959.2:c.*1527A=	NP_001076428.1:n.*1527A=
NM_001367981.1:c.*1639A=	NP_001354910.1:n.*1639A=
NM_001367983.1:c.*1647A=	NP_001354912.1:n.*1647A=
NM_001367984.1:c.*1647A=	NP_001354913.1:n.*1647A=
NM_001367985.1:c.*1647A=	NP_001354914.1:n.*1647A=
NM_001367986.1:c.*1647A=	NP_001354915.1:n.*1647A=
NM_001367987.1:c.*1527A=	NP_001354916.1:n.*1527A=
NM_001367988.1:c.*1647A=	NP_001354917.1:n.*1647A=
NM_001367989.1:c.*1658A=	NP_001354918.1:n.*1658A=
NR_160416.1:n.3322A=
NR_160417.1:n.3424A=
NR_160418.1:n.2883A=
NR_160419.1:n.3247A=
NR_160420.1:n.3076A=
NR_160421.1:n.2999A=
NR_160422.1:n.3205A=
NR_160423.1:n.3202A=
NR_160424.1:n.3187A=