Canonical Allele Identifier: CA552873273

Gene: ABCG2

Linked Data

• dbSNP Id: rs1231857468
• gnomAD v2: 4-89068202-G-GAAAGAAAGAAAGAAAGAAAGA
• gnomAD v3: 4-88147050-G-GAAAGAAAGAAAGAAAGAAAGA
• gnomAD v4: 4-88147050-G-GAAAGAAAGAAAGAAAGAAAGA
• MyVariant Identifiers: chr4:g.89068202_89068203insAAAGAAAGAAAGAAAGAAAGA (hg19) ; chr4:g.88147050_88147051insAAAGAAAGAAAGAAAGAAAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88147054_88147055insAAAGAAAGAAAGAAAGAAAAG , CM000666.2:g.88147054_88147055insAAAGAAAGAAAGAAAGAAAAG	GRCh38
NC_000004.11:g.89068206_89068207insAAAGAAAGAAAGAAAGAAAAG , CM000666.1:g.89068206_89068207insAAAGAAAGAAAGAAAGAAAAG	GRCh37
NC_000004.10:g.89287230_89287231insAAAGAAAGAAAGAAAGAAAAG	NCBI36
NG_032067.2:g.89272_89273insTCTTTCTTTCTTTCTTTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT MANE Select	ENSP00000237612.3:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT...
ENST00000503830.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000426934.2:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT...
ENST00000505480.6:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000426916.2:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT...
ENST00000650821.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000498246.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT...
ENST00000237612.7:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000237612.3:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT...
ENST00000503830.1:c.36-7037_36-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000426934.1:n.36-7037_36-7036insTCTTTCTTTCTTTCTTTCTTT
ENST00000505480.5:c.96-7037_96-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000426916.1:n.96-7037_96-7036insTCTTTCTTTCTTTCTTTCTTT
ENST00000515655.5:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	ENSP00000426917.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT...
NM_001257386.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001244315.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_004827.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_004818.2:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_005263354.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_005263411.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_005263355.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_005263412.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_005263356.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_005263413.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_011532420.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_011530722.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_001257386.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001244315.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_001348985.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001335914.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_001348986.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001335915.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_001348987.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001335916.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_001348988.1:c.-20+3141_-20+3142insTCTTTCTTTCTTTCTTTCTTT	NP_001335917.1:n.-20+3141_-20+3142insTCTTTCTTTCTTTCTTTCTTT
NM_001348989.1:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001335918.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_005263355.4:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_005263412.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_011532420.3:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_011530722.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
XM_017008852.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	XP_016864341.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_004827.3:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT MANE Select	NP_004818.2:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT
NM_001348989.2:c.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT	NP_001335918.1:n.-19-7037_-19-7036insTCTTTCTTTCTTTCTTTCTTT