Canonical Allele Identifier: CA552873250

Gene: ABCG2

Linked Data

• dbSNP Id: rs1394396531
• gnomAD v2: 4-89068171-A-AAGAAAGAAAGAAAGAAAGAAAGAAAG
• gnomAD v3: 4-88147019-A-AAGAAAGAAAGAAAGAAAGAAAGAAAG
• gnomAD v4: 4-88147019-A-AAGAAAGAAAGAAAGAAAGAAAGAAAG
• MyVariant Identifiers: chr4:g.89068171_89068172insAGAAAGAAAGAAAGAAAGAAAGAAAG (hg19) ; chr4:g.88147019_88147020insAGAAAGAAAGAAAGAAAGAAAGAAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88147021_88147046dup , CM000666.2:g.88147021_88147046dup	GRCh38
NC_000004.11:g.89068173_89068198dup , CM000666.1:g.89068173_89068198dup	GRCh37
NC_000004.10:g.89287197_89287222dup	NCBI36
NG_032067.2:g.89278_89303dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000237612.8:c.-19-7031_-19-7006dup MANE Select	ENSP00000237612.3:n.-19-7031_-19-7006dup
ENST00000503830.2:c.-19-7031_-19-7006dup	ENSP00000426934.2:n.-19-7031_-19-7006dup
ENST00000505480.6:c.-19-7031_-19-7006dup	ENSP00000426916.2:n.-19-7031_-19-7006dup
ENST00000650821.1:c.-19-7031_-19-7006dup	ENSP00000498246.1:n.-19-7031_-19-7006dup
ENST00000237612.7:c.-19-7031_-19-7006dup	ENSP00000237612.3:n.-19-7031_-19-7006dup
ENST00000503830.1:c.36-7031_36-7006dup	ENSP00000426934.1:n.36-7031_36-7006dup
ENST00000505480.5:c.96-7031_96-7006dup	ENSP00000426916.1:n.96-7031_96-7006dup
ENST00000515655.5:c.-19-7031_-19-7006dup	ENSP00000426917.1:n.-19-7031_-19-7006dup
NM_001257386.1:c.-19-7031_-19-7006dup	NP_001244315.1:n.-19-7031_-19-7006dup
NM_004827.2:c.-19-7031_-19-7006dup	NP_004818.2:n.-19-7031_-19-7006dup
XM_005263354.2:c.-19-7031_-19-7006dup	XP_005263411.1:n.-19-7031_-19-7006dup
XM_005263355.2:c.-19-7031_-19-7006dup	XP_005263412.1:n.-19-7031_-19-7006dup
XM_005263356.2:c.-19-7031_-19-7006dup	XP_005263413.1:n.-19-7031_-19-7006dup
XM_011532420.1:c.-19-7031_-19-7006dup	XP_011530722.1:n.-19-7031_-19-7006dup
NM_001257386.2:c.-19-7031_-19-7006dup	NP_001244315.1:n.-19-7031_-19-7006dup
NM_001348985.1:c.-19-7031_-19-7006dup	NP_001335914.1:n.-19-7031_-19-7006dup
NM_001348986.1:c.-19-7031_-19-7006dup	NP_001335915.1:n.-19-7031_-19-7006dup
NM_001348987.1:c.-19-7031_-19-7006dup	NP_001335916.1:n.-19-7031_-19-7006dup
NM_001348988.1:c.-20+3147_-20+3172dup	NP_001335917.1:n.-20+3147_-20+3172dup
NM_001348989.1:c.-19-7031_-19-7006dup	NP_001335918.1:n.-19-7031_-19-7006dup
XM_005263355.4:c.-19-7031_-19-7006dup	XP_005263412.1:n.-19-7031_-19-7006dup
XM_011532420.3:c.-19-7031_-19-7006dup	XP_011530722.1:n.-19-7031_-19-7006dup
XM_017008852.2:c.-19-7031_-19-7006dup	XP_016864341.1:n.-19-7031_-19-7006dup
NM_004827.3:c.-19-7031_-19-7006dup MANE Select	NP_004818.2:n.-19-7031_-19-7006dup
NM_001348989.2:c.-19-7031_-19-7006dup	NP_001335918.1:n.-19-7031_-19-7006dup