Canonical Allele Identifier: CA1474627582

Gene: ABCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88157772T= , CM000666.2:g.88157772T=	GRCh38
NC_000004.11:g.89078924T= , CM000666.1:g.89078924T=	GRCh37
NC_000004.10:g.89297948T=	NCBI36
NG_032067.2:g.78551A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004827.3:c.-20+614A= MANE Select	NP_004818.2:n.-20+614A=
ENST00000237612.8:c.-20+614A= MANE Select	ENSP00000237612.3:n.-20+614A=
NM_001257386.1:c.-19-17758A=	NP_001244315.1:n.-19-17758A=
NM_001257386.2:c.-19-17758A=	NP_001244315.1:n.-19-17758A=
NM_001348985.1:c.-19-17758A=	NP_001335914.1:n.-19-17758A=
NM_001348986.1:c.-20+805A=	NP_001335915.1:n.-20+805A=
NM_001348987.1:c.-20+614A=	NP_001335916.1:n.-20+614A=
NM_001348988.1:c.-214+614A=	NP_001335917.1:n.-214+614A=
NM_001348989.1:c.-20+1433A=	NP_001335918.1:n.-20+1433A=
NM_001348989.2:c.-20+1433A=	NP_001335918.1:n.-20+1433A=
NM_004827.2:c.-20+614A=	NP_004818.2:n.-20+614A=
ENST00000237612.7:c.-20+614A=	ENSP00000237612.3:n.-20+614A=
ENST00000503830.1:c.35+1433A=	ENSP00000426934.1:n.35+1433A=
ENST00000503830.2:c.-20+1433A=	ENSP00000426934.2:n.-20+1433A=
ENST00000505480.5:c.95+805A=	ENSP00000426916.1:n.95+805A=
ENST00000505480.6:c.-20+805A=	ENSP00000426916.2:n.-20+805A=
ENST00000515655.5:c.-19-17758A=	ENSP00000426917.1:n.-19-17758A=
ENST00000650821.1:c.-19-17758A=	ENSP00000498246.1:n.-19-17758A=
XM_005263354.2:c.-20+805A=	XP_005263411.1:n.-20+805A=
XM_005263355.2:c.-19-17758A=	XP_005263412.1:n.-19-17758A=
XM_005263355.4:c.-19-17758A=	XP_005263412.1:n.-19-17758A=
XM_005263356.2:c.-20+614A=	XP_005263413.1:n.-20+614A=
XM_011532420.1:c.-19-17758A=	XP_011530722.1:n.-19-17758A=
XM_011532420.3:c.-19-17758A=	XP_011530722.1:n.-19-17758A=
XM_017008852.2:c.-20+805A=	XP_016864341.1:n.-20+805A=