Canonical Allele Identifier: CA799621048

Gene: ABCG2

Linked Data

• dbSNP Id: rs1280776082
• gnomAD v3: 4-88146893-G-GAGAA
• gnomAD v4: 4-88146893-G-GAGAA
• MyVariant Identifiers: chr4:g.89068045_89068046insAGAA (hg19) ; chr4:g.88146893_88146894insAGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88146898_88146901dup , CM000666.2:g.88146898_88146901dup	GRCh38
NC_000004.11:g.89068050_89068053dup , CM000666.1:g.89068050_89068053dup	GRCh37
NC_000004.10:g.89287074_89287077dup	NCBI36
NG_032067.2:g.89426_89429dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.-19-6883_-19-6880dup MANE Select	ENSP00000237612.3:n.-19-6883_-19-6880dup
ENST00000503830.2:c.-19-6883_-19-6880dup	ENSP00000426934.2:n.-19-6883_-19-6880dup
ENST00000505480.6:c.-19-6883_-19-6880dup	ENSP00000426916.2:n.-19-6883_-19-6880dup
ENST00000650821.1:c.-19-6883_-19-6880dup	ENSP00000498246.1:n.-19-6883_-19-6880dup
ENST00000237612.7:c.-19-6883_-19-6880dup	ENSP00000237612.3:n.-19-6883_-19-6880dup
ENST00000503830.1:c.36-6883_36-6880dup	ENSP00000426934.1:n.36-6883_36-6880dup
ENST00000505480.5:c.96-6883_96-6880dup	ENSP00000426916.1:n.96-6883_96-6880dup
ENST00000515655.5:c.-19-6883_-19-6880dup	ENSP00000426917.1:n.-19-6883_-19-6880dup
NM_001257386.1:c.-19-6883_-19-6880dup	NP_001244315.1:n.-19-6883_-19-6880dup
NM_004827.2:c.-19-6883_-19-6880dup	NP_004818.2:n.-19-6883_-19-6880dup
XM_005263354.2:c.-19-6883_-19-6880dup	XP_005263411.1:n.-19-6883_-19-6880dup
XM_005263355.2:c.-19-6883_-19-6880dup	XP_005263412.1:n.-19-6883_-19-6880dup
XM_005263356.2:c.-19-6883_-19-6880dup	XP_005263413.1:n.-19-6883_-19-6880dup
XM_011532420.1:c.-19-6883_-19-6880dup	XP_011530722.1:n.-19-6883_-19-6880dup
NM_001257386.2:c.-19-6883_-19-6880dup	NP_001244315.1:n.-19-6883_-19-6880dup
NM_001348985.1:c.-19-6883_-19-6880dup	NP_001335914.1:n.-19-6883_-19-6880dup
NM_001348986.1:c.-19-6883_-19-6880dup	NP_001335915.1:n.-19-6883_-19-6880dup
NM_001348987.1:c.-19-6883_-19-6880dup	NP_001335916.1:n.-19-6883_-19-6880dup
NM_001348988.1:c.-20+3295_-20+3298dup	NP_001335917.1:n.-20+3295_-20+3298dup
NM_001348989.1:c.-19-6883_-19-6880dup	NP_001335918.1:n.-19-6883_-19-6880dup
XM_005263355.4:c.-19-6883_-19-6880dup	XP_005263412.1:n.-19-6883_-19-6880dup
XM_011532420.3:c.-19-6883_-19-6880dup	XP_011530722.1:n.-19-6883_-19-6880dup
XM_017008852.2:c.-19-6883_-19-6880dup	XP_016864341.1:n.-19-6883_-19-6880dup
NM_004827.3:c.-19-6883_-19-6880dup MANE Select	NP_004818.2:n.-19-6883_-19-6880dup
NM_001348989.2:c.-19-6883_-19-6880dup	NP_001335918.1:n.-19-6883_-19-6880dup