Canonical Allele Identifier: CA2390699942

Gene: ABCG1 RNA5SP492

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42221237G= , CM000683.2:g.42221237G=	GRCh38
NC_000021.8:g.43641347G= , CM000683.1:g.43641347G=	GRCh37
NC_000021.7:g.42514416G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016818.3:c.42+1933G= (ABCG1) MANE Select	NP_058198.2:n.42+1933G=
ENST00000398449.8:c.42+1933G= (ABCG1) MANE Select	ENSP00000381467.3:n.42+1933G=
NM_004915.3:c.42+1933G= (ABCG1)	NP_004906.3:n.42+1933G=
NM_004915.4:c.42+1933G= (ABCG1)	NP_004906.3:n.42+1933G=
NM_016818.2:c.42+1933G= (ABCG1)	NP_058198.2:n.42+1933G=
NM_207174.1:c.75+1191G= (ABCG1)	NP_997057.1:n.75+1191G=
NM_207627.1:c.49-4434G= (ABCG1)	NP_997510.1:n.49-4434G=
NM_207627.2:c.49-4434G= (ABCG1)	NP_997510.1:n.49-4434G=
NM_207628.1:c.-24-4434G= (ABCG1)	NP_997511.1:n.-24-4434G=
NM_207629.1:c.34-4434G= (ABCG1)	NP_997512.1:n.34-4434G=
NM_207629.2:c.34-4434G= (ABCG1)	NP_997512.1:n.34-4434G=
ENST00000343687.7:c.75+1191G= (ABCG1)	ENSP00000339744.3:n.75+1191G=
ENST00000347800.6:c.34-4434G= (ABCG1)	ENSP00000291524.4:n.34-4434G=
ENST00000361802.6:c.42+1933G= (ABCG1)	ENSP00000354995.2:n.42+1933G=
ENST00000398449.7:c.42+1933G= (ABCG1)	ENSP00000381467.3:n.42+1933G=
ENST00000398457.6:c.49-4434G= (ABCG1)	ENSP00000381475.2:n.49-4434G=
ENST00000411330.1:n.65G= (RNA5SP492)
ENST00000450121.5:c.42+1933G= (ABCG1)	ENSP00000414541.1:n.42+1933G=
ENST00000462050.5:n.227-4434G= (ABCG1)
XM_011529806.1:c.75+1191G= (ABCG1)	XP_011528108.1:n.75+1191G=
XM_011529807.1:c.75+1191G= (ABCG1)	XP_011528109.1:n.75+1191G=
XM_011529807.3:c.75+1191G= (ABCG1)	XP_011528109.1:n.75+1191G=
XR_937748.1:n.1657C=
XR_937748.3:n.4425C=