Canonical Allele Identifier: CA2390730790

Gene: ABCG1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42286991C= , CM000683.2:g.42286991C=	GRCh38
NC_000021.8:g.43707101C= , CM000683.1:g.43707101C=	GRCh37
NC_000021.7:g.42580170C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016818.3:c.974-898C= MANE Select	NP_058198.2:n.974-898C=
ENST00000398449.8:c.974-898C= MANE Select	ENSP00000381467.3:n.974-898C=
NM_004915.3:c.974-898C=	NP_004906.3:n.974-898C=
NM_004915.4:c.974-898C=	NP_004906.3:n.974-898C=
NM_016818.2:c.974-898C=	NP_058198.2:n.974-898C=
NM_207174.1:c.1007-898C=	NP_997057.1:n.1007-898C=
NM_207627.1:c.980-898C=	NP_997510.1:n.980-898C=
NM_207627.2:c.980-898C=	NP_997510.1:n.980-898C=
NM_207628.1:c.908-898C=	NP_997511.1:n.908-898C=
NM_207629.1:c.965-898C=	NP_997512.1:n.965-898C=
NM_207629.2:c.965-898C=	NP_997512.1:n.965-898C=
ENST00000343687.7:c.1007-898C=	ENSP00000339744.3:n.1007-898C=
ENST00000347800.6:c.965-898C=	ENSP00000291524.4:n.965-898C=
ENST00000361802.6:c.974-898C=	ENSP00000354995.2:n.974-898C=
ENST00000398437.1:c.1412-898C=	ENSP00000381464.1:n.1412-898C=
ENST00000398449.7:c.974-898C=	ENSP00000381467.3:n.974-898C=
ENST00000398457.6:c.980-898C=	ENSP00000381475.2:n.980-898C=
ENST00000462050.5:n.1158-898C=
ENST00000472587.5:n.988-898C=
ENST00000496783.1:n.62-898C=
XM_011529806.1:c.1007-898C=	XP_011528108.1:n.1007-898C=
XM_011529807.1:c.1007-898C=	XP_011528109.1:n.1007-898C=
XM_011529807.3:c.1007-898C=	XP_011528109.1:n.1007-898C=
XM_024452141.1:c.1298-898C=	XP_024307909.1:n.1298-898C=