Canonical Allele Identifier: CA799621136

Gene: ABCG2

Linked Data

• dbSNP Id: rs1196059568
• MyVariant Identifiers: chr4:g.89068083_89068084insAGGG (hg19) ; chr4:g.88146931_88146932insAGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88146934_88146935insGAGG , CM000666.2:g.88146934_88146935insGAGG	GRCh38
NC_000004.11:g.89068086_89068087insGAGG , CM000666.1:g.89068086_89068087insGAGG	GRCh37
NC_000004.10:g.89287110_89287111insGAGG	NCBI36
NG_032067.2:g.89391_89392insCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.-19-6918_-19-6917insCCCT MANE Select	ENSP00000237612.3:n.-19-6918_-19-6917insCCCT
ENST00000503830.2:c.-19-6918_-19-6917insCCCT	ENSP00000426934.2:n.-19-6918_-19-6917insCCCT
ENST00000505480.6:c.-19-6918_-19-6917insCCCT	ENSP00000426916.2:n.-19-6918_-19-6917insCCCT
ENST00000650821.1:c.-19-6918_-19-6917insCCCT	ENSP00000498246.1:n.-19-6918_-19-6917insCCCT
ENST00000237612.7:c.-19-6918_-19-6917insCCCT	ENSP00000237612.3:n.-19-6918_-19-6917insCCCT
ENST00000503830.1:c.36-6918_36-6917insCCCT	ENSP00000426934.1:n.36-6918_36-6917insCCCT
ENST00000505480.5:c.96-6918_96-6917insCCCT	ENSP00000426916.1:n.96-6918_96-6917insCCCT
ENST00000515655.5:c.-19-6918_-19-6917insCCCT	ENSP00000426917.1:n.-19-6918_-19-6917insCCCT
NM_001257386.1:c.-19-6918_-19-6917insCCCT	NP_001244315.1:n.-19-6918_-19-6917insCCCT
NM_004827.2:c.-19-6918_-19-6917insCCCT	NP_004818.2:n.-19-6918_-19-6917insCCCT
XM_005263354.2:c.-19-6918_-19-6917insCCCT	XP_005263411.1:n.-19-6918_-19-6917insCCCT
XM_005263355.2:c.-19-6918_-19-6917insCCCT	XP_005263412.1:n.-19-6918_-19-6917insCCCT
XM_005263356.2:c.-19-6918_-19-6917insCCCT	XP_005263413.1:n.-19-6918_-19-6917insCCCT
XM_011532420.1:c.-19-6918_-19-6917insCCCT	XP_011530722.1:n.-19-6918_-19-6917insCCCT
NM_001257386.2:c.-19-6918_-19-6917insCCCT	NP_001244315.1:n.-19-6918_-19-6917insCCCT
NM_001348985.1:c.-19-6918_-19-6917insCCCT	NP_001335914.1:n.-19-6918_-19-6917insCCCT
NM_001348986.1:c.-19-6918_-19-6917insCCCT	NP_001335915.1:n.-19-6918_-19-6917insCCCT
NM_001348987.1:c.-19-6918_-19-6917insCCCT	NP_001335916.1:n.-19-6918_-19-6917insCCCT
NM_001348988.1:c.-20+3260_-20+3261insCCCT	NP_001335917.1:n.-20+3260_-20+3261insCCCT
NM_001348989.1:c.-19-6918_-19-6917insCCCT	NP_001335918.1:n.-19-6918_-19-6917insCCCT
XM_005263355.4:c.-19-6918_-19-6917insCCCT	XP_005263412.1:n.-19-6918_-19-6917insCCCT
XM_011532420.3:c.-19-6918_-19-6917insCCCT	XP_011530722.1:n.-19-6918_-19-6917insCCCT
XM_017008852.2:c.-19-6918_-19-6917insCCCT	XP_016864341.1:n.-19-6918_-19-6917insCCCT
NM_004827.3:c.-19-6918_-19-6917insCCCT MANE Select	NP_004818.2:n.-19-6918_-19-6917insCCCT
NM_001348989.2:c.-19-6918_-19-6917insCCCT	NP_001335918.1:n.-19-6918_-19-6917insCCCT