Canonical Allele Identifier: CA1474623399

Gene: ABCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88147000_88147005delinsAGAAAG , CM000666.2:g.88147000_88147005delinsAGAAAG	GRCh38
NC_000004.11:g.89068152_89068157delinsAGAAAG , CM000666.1:g.89068152_89068157delinsAGAAAG	GRCh37
NC_000004.10:g.89287176_89287181delinsAGAAAG	NCBI36
NG_032067.2:g.89318_89323delinsCTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.-19-6991_-19-6986delinsCTTTCT MANE Select	ENSP00000237612.3:n.-19-6991_-19-6986delinsCTTTCT
ENST00000503830.2:c.-19-6991_-19-6986delinsCTTTCT	ENSP00000426934.2:n.-19-6991_-19-6986delinsCTTTCT
ENST00000505480.6:c.-19-6991_-19-6986delinsCTTTCT	ENSP00000426916.2:n.-19-6991_-19-6986delinsCTTTCT
ENST00000650821.1:c.-19-6991_-19-6986delinsCTTTCT	ENSP00000498246.1:n.-19-6991_-19-6986delinsCTTTCT
ENST00000237612.7:c.-19-6991_-19-6986delinsCTTTCT	ENSP00000237612.3:n.-19-6991_-19-6986delinsCTTTCT
ENST00000503830.1:c.36-6991_36-6986delinsCTTTCT	ENSP00000426934.1:n.36-6991_36-6986delinsCTTTCT
ENST00000505480.5:c.96-6991_96-6986delinsCTTTCT	ENSP00000426916.1:n.96-6991_96-6986delinsCTTTCT
ENST00000515655.5:c.-19-6991_-19-6986delinsCTTTCT	ENSP00000426917.1:n.-19-6991_-19-6986delinsCTTTCT
NM_001257386.1:c.-19-6991_-19-6986delinsCTTTCT	NP_001244315.1:n.-19-6991_-19-6986delinsCTTTCT
NM_004827.2:c.-19-6991_-19-6986delinsCTTTCT	NP_004818.2:n.-19-6991_-19-6986delinsCTTTCT
XM_005263354.2:c.-19-6991_-19-6986delinsCTTTCT	XP_005263411.1:n.-19-6991_-19-6986delinsCTTTCT
XM_005263355.2:c.-19-6991_-19-6986delinsCTTTCT	XP_005263412.1:n.-19-6991_-19-6986delinsCTTTCT
XM_005263356.2:c.-19-6991_-19-6986delinsCTTTCT	XP_005263413.1:n.-19-6991_-19-6986delinsCTTTCT
XM_011532420.1:c.-19-6991_-19-6986delinsCTTTCT	XP_011530722.1:n.-19-6991_-19-6986delinsCTTTCT
NM_001257386.2:c.-19-6991_-19-6986delinsCTTTCT	NP_001244315.1:n.-19-6991_-19-6986delinsCTTTCT
NM_001348985.1:c.-19-6991_-19-6986delinsCTTTCT	NP_001335914.1:n.-19-6991_-19-6986delinsCTTTCT
NM_001348986.1:c.-19-6991_-19-6986delinsCTTTCT	NP_001335915.1:n.-19-6991_-19-6986delinsCTTTCT
NM_001348987.1:c.-19-6991_-19-6986delinsCTTTCT	NP_001335916.1:n.-19-6991_-19-6986delinsCTTTCT
NM_001348988.1:c.-20+3187_-20+3192delinsCTTTCT	NP_001335917.1:n.-20+3187_-20+3192delinsCTTTCT
NM_001348989.1:c.-19-6991_-19-6986delinsCTTTCT	NP_001335918.1:n.-19-6991_-19-6986delinsCTTTCT
XM_005263355.4:c.-19-6991_-19-6986delinsCTTTCT	XP_005263412.1:n.-19-6991_-19-6986delinsCTTTCT
XM_011532420.3:c.-19-6991_-19-6986delinsCTTTCT	XP_011530722.1:n.-19-6991_-19-6986delinsCTTTCT
XM_017008852.2:c.-19-6991_-19-6986delinsCTTTCT	XP_016864341.1:n.-19-6991_-19-6986delinsCTTTCT
NM_004827.3:c.-19-6991_-19-6986delinsCTTTCT MANE Select	NP_004818.2:n.-19-6991_-19-6986delinsCTTTCT
NM_001348989.2:c.-19-6991_-19-6986delinsCTTTCT	NP_001335918.1:n.-19-6991_-19-6986delinsCTTTCT