Canonical Allele Identifier: CA2390736052

Gene: ABCG1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42296618T= , CM000683.2:g.42296618T=	GRCh38
NC_000021.8:g.43716728T= , CM000683.1:g.43716728T=	GRCh37
NC_000021.7:g.42589797T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398449.8:c.*226T= MANE Select	ENSP00000381467.3:n.*226T=
ENST00000343687.7:c.*226T=	ENSP00000339744.3:n.*226T=
ENST00000347800.6:c.*226T=	ENSP00000291524.4:n.*226T=
ENST00000361802.6:c.*226T=	ENSP00000354995.2:n.*226T=
ENST00000398437.1:c.*226T=	ENSP00000381464.1:n.*226T=
ENST00000398449.7:c.*226T=	ENSP00000381467.3:n.*226T=
ENST00000398457.6:c.*226T=	ENSP00000381475.2:n.*226T=
ENST00000462050.5:n.2411T=
ENST00000472587.5:n.2277T=
NM_004915.3:c.*226T=	NP_004906.3:n.*226T=
NM_016818.2:c.*226T=	NP_058198.2:n.*226T=
NM_207174.1:c.*226T=	NP_997057.1:n.*226T=
NM_207627.1:c.*226T=	NP_997510.1:n.*226T=
NM_207628.1:c.*226T=	NP_997511.1:n.*226T=
NM_207629.1:c.*226T=	NP_997512.1:n.*226T=
XM_011529806.1:c.*226T=	XP_011528108.1:n.*226T=
XM_011529807.1:c.*392T=	XP_011528109.1:n.*392T=
XM_011529807.3:c.*392T=	XP_011528109.1:n.*392T=
XM_024452141.1:c.*226T=	XP_024307909.1:n.*226T=
NM_004915.4:c.*226T=	NP_004906.3:n.*226T=
NM_016818.3:c.*226T= MANE Select	NP_058198.2:n.*226T=
NM_207627.2:c.*226T=	NP_997510.1:n.*226T=
NM_207629.2:c.*226T=	NP_997512.1:n.*226T=