Canonical Allele Identifier: CA2069464198

Gene: SCARB1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124776945T= , CM000674.2:g.124776945T=	GRCh38
NC_000012.11:g.125261491T= , CM000674.1:g.125261491T=	GRCh37
NC_000012.10:g.123827444T=	NCBI36
NG_028199.1:g.92029A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261693.11:c.*1642A= MANE Select	ENSP00000261693.6:n.*1642A=
ENST00000339570.9:c.*1522A=	ENSP00000343795.4:n.*1522A=
NM_005505.5:c.*1642A= MANE Select	NP_005496.4:n.*1642A=
NM_001082959.2:c.*1522A=	NP_001076428.1:n.*1522A=
NM_001367981.1:c.*1634A=	NP_001354910.1:n.*1634A=
NM_001367983.1:c.*1642A=	NP_001354912.1:n.*1642A=
NM_001367984.1:c.*1642A=	NP_001354913.1:n.*1642A=
NM_001367985.1:c.*1642A=	NP_001354914.1:n.*1642A=
NM_001367986.1:c.*1642A=	NP_001354915.1:n.*1642A=
NM_001367987.1:c.*1522A=	NP_001354916.1:n.*1522A=
NM_001367988.1:c.*1642A=	NP_001354917.1:n.*1642A=
NM_001367989.1:c.*1653A=	NP_001354918.1:n.*1653A=
NR_160416.1:n.3317A=
NR_160417.1:n.3419A=
NR_160418.1:n.2878A=
NR_160419.1:n.3242A=
NR_160420.1:n.3071A=
NR_160421.1:n.2994A=
NR_160422.1:n.3200A=
NR_160423.1:n.3197A=
NR_160424.1:n.3182A=