Canonical Allele Identifier: CA1474623508

Gene: ABCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88147070_88147080delinsGGAAAAGAAAA , CM000666.2:g.88147070_88147080delinsGGAAAAGAAAA	GRCh38
NC_000004.11:g.89068222_89068232delinsGGAAAAGAAAA , CM000666.1:g.89068222_89068232delinsGGAAAAGAAAA	GRCh37
NC_000004.10:g.89287246_89287256delinsGGAAAAGAAAA	NCBI36
NG_032067.2:g.89243_89253delinsTTTTCTTTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.-19-7066_-19-7056delinsTTTTCTTTTCC MANE Select	ENSP00000237612.3:n.-19-7066_-19-7056delinsTTTTCTTTTCC
ENST00000503830.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	ENSP00000426934.2:n.-19-7066_-19-7056delinsTTTTCTTTTCC
ENST00000505480.6:c.-19-7066_-19-7056delinsTTTTCTTTTCC	ENSP00000426916.2:n.-19-7066_-19-7056delinsTTTTCTTTTCC
ENST00000650821.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	ENSP00000498246.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
ENST00000237612.7:c.-19-7066_-19-7056delinsTTTTCTTTTCC	ENSP00000237612.3:n.-19-7066_-19-7056delinsTTTTCTTTTCC
ENST00000503830.1:c.36-7066_36-7056delinsTTTTCTTTTCC	ENSP00000426934.1:n.36-7066_36-7056delinsTTTTCTTTTCC
ENST00000505480.5:c.96-7066_96-7056delinsTTTTCTTTTCC	ENSP00000426916.1:n.96-7066_96-7056delinsTTTTCTTTTCC
ENST00000515655.5:c.-19-7066_-19-7056delinsTTTTCTTTTCC	ENSP00000426917.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001257386.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001244315.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_004827.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_004818.2:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_005263354.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_005263411.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_005263355.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_005263412.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_005263356.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_005263413.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_011532420.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_011530722.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001257386.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001244315.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001348985.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001335914.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001348986.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001335915.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001348987.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001335916.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001348988.1:c.-20+3112_-20+3122delinsTTTTCTTTTCC	NP_001335917.1:n.-20+3112_-20+3122delinsTTTTCTTTTCC
NM_001348989.1:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001335918.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_005263355.4:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_005263412.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_011532420.3:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_011530722.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
XM_017008852.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	XP_016864341.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_004827.3:c.-19-7066_-19-7056delinsTTTTCTTTTCC MANE Select	NP_004818.2:n.-19-7066_-19-7056delinsTTTTCTTTTCC
NM_001348989.2:c.-19-7066_-19-7056delinsTTTTCTTTTCC	NP_001335918.1:n.-19-7066_-19-7056delinsTTTTCTTTTCC