Canonical Allele Identifier: CA1474616670

Gene: ABCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88131171G= , CM000666.2:g.88131171G=	GRCh38
NC_000004.11:g.89052323G= , CM000666.1:g.89052323G=	GRCh37
NC_000004.10:g.89271347G=	NCBI36
NG_032067.2:g.105152C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237612.8:c.421C= MANE Select	ENSP00000237612.3:p.Gln141=
ENST00000650821.1:c.421C=	ENSP00000498246.1:p.Gln141=
ENST00000237612.7:c.421C=	ENSP00000237612.3:p.Gln141=
ENST00000515655.5:c.421C=	ENSP00000426917.1:p.Gln141=
NM_001257386.1:c.421C=	NP_001244315.1:p.Gln141=
NM_004827.2:c.421C=	NP_004818.2:p.Gln141=
XM_005263354.2:c.421C=	XP_005263411.1:p.Gln141=
XM_005263355.2:c.421C=	XP_005263412.1:p.Gln141=
XM_005263356.2:c.421C=	XP_005263413.1:p.Gln141=
XM_011532420.1:c.421C=	XP_011530722.1:p.Gln141=
NM_001257386.2:c.421C=	NP_001244315.1:p.Gln141=
NM_001348985.1:c.421C=	NP_001335914.1:p.Gln141=
NM_001348986.1:c.421C=	NP_001335915.1:p.Gln141=
NM_001348987.1:c.421C=	NP_001335916.1:p.Gln141=
NM_001348988.1:c.421C=	NP_001335917.1:p.Gln141=
NM_001348989.1:c.421C=	NP_001335918.1:p.Gln141=
XM_005263355.4:c.421C=	XP_005263412.1:p.Gln141=
XM_011532420.3:c.421C=	XP_011530722.1:p.Gln141=
XM_017008852.2:c.421C=	XP_016864341.1:p.Gln141=
NM_004827.3:c.421C= MANE Select	NP_004818.2:p.Gln141=
NM_001348989.2:c.421C=	NP_001335918.1:p.Gln141=