Canonical Allele Identifier: CA1413086913

Gene: SLC33A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.155854059A= , CM000665.2:g.155854059A=	GRCh38
NC_000003.11:g.155571848A= , CM000665.1:g.155571848A=	GRCh37
NC_000003.10:g.157054542A=	NCBI36
NG_023365.1:g.5401T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468581.2:c.-62T=	ENSP00000418847.2:n.-62T=
ENST00000642438.1:c.-62T=	ENSP00000495971.1:n.-62T=
ENST00000643144.2:c.-62T= MANE Select	ENSP00000496241.1:n.-62T=
ENST00000643876.1:c.-62T=	ENSP00000495323.1:n.-62T=
ENST00000644094.1:c.-62T=	ENSP00000494476.1:n.-62T=
ENST00000644855.1:c.-62T=	ENSP00000493564.1:n.-62T=
ENST00000646424.1:c.-62T=	ENSP00000494846.1:n.-62T=
ENST00000359479.7:c.-62T=	ENSP00000352456.3:n.-62T=
ENST00000392845.7:c.-62T=	ENSP00000376587.2:n.-62T=
NM_001190992.1:c.-62T=	NP_001177921.1:n.-62T=
NM_004733.3:c.-62T=	NP_004724.1:n.-62T=
XM_006713822.2:c.-62T=	XP_006713885.1:n.-62T=
XM_011513311.1:c.-62T=	XP_011511613.1:n.-62T=
XM_011513312.1:c.-62T=	XP_011511614.1:n.-62T=
NM_001363883.1:c.-62T=	NP_001350812.1:n.-62T=
XM_011513311.3:c.-62T=	XP_011511613.1:n.-62T=
XM_017007463.1:c.-687T=	XP_016862952.1:n.-687T=
XM_017007464.1:c.-687T=	XP_016862953.1:n.-687T=
XR_001740361.2:n.1300T=
XR_001740362.2:n.1300T=
XR_002959605.1:n.1300T=
NM_004733.4:c.-62T= MANE Select	NP_004724.1:n.-62T=
NM_001190992.2:c.-62T=	NP_001177921.1:n.-62T=