Canonical Allele Identifier: CA2033475679

Gene: ARID2

Linked Data

• dbSNP Id: rs1943574799

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852570_45852571insATTCTT , CM000674.2:g.45852570_45852571insATTCTT	GRCh38
NC_000012.11:g.46246353_46246354insATTCTT , CM000674.1:g.46246353_46246354insATTCTT	GRCh37
NC_000012.10:g.44532620_44532621insATTCTT	NCBI36
NG_052800.1:g.127906_127907insATTCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000422737.7:c.4447_4448insATTCTT	ENSP00000415650.3:p.Ile1483delinsAsnSerPhe
ENST00000457135.2:c.656_657insATTCTT
ENST00000334344.11:c.4447_4448insATTCTT MANE Select	ENSP00000335044.6:p.Ile1483delinsAsnSerPhe
ENST00000422737.6:c.4368_4369insATTCTT
ENST00000334344.10:c.4447_4448insATTCTT	ENSP00000335044.6:p.Ile1483delinsAsnSerPhe
ENST00000422737.5:c.4000_4001insATTCTT	ENSP00000415650.1:p.Ile1334delinsAsnSerPhe
ENST00000444670.5:c.3277_3278insATTCTT	ENSP00000397307.1:p.Ile1093delinsAsnSerPhe
ENST00000457135.1:c.271_272insATTCTT	ENSP00000388357.1:p.Ile91delinsAsnSerPhe
ENST00000479608.5:n.3738_3739insATTCTT
NM_152641.2:c.4447_4448insATTCTT	NP_689854.2:p.Ile1483delinsAsnSerPhe
XM_006719272.2:c.4447_4448insATTCTT	XP_006719335.1:p.Ile1483delinsAsnSerPhe
XM_011538025.1:c.2815_2816insATTCTT	XP_011536327.1:p.Ile939delinsAsnSerPhe
XR_944505.1:n.4595_4596insATTCTT
NM_001347839.1:c.4447_4448insATTCTT	NP_001334768.1:p.Ile1483delinsAsnSerPhe
NM_152641.3:c.4447_4448insATTCTT	NP_689854.2:p.Ile1483delinsAsnSerPhe
XM_006719272.4:c.4447_4448insATTCTT	XP_006719335.1:p.Ile1483delinsAsnSerPhe
XR_944505.3:n.4578_4579insATTCTT
NM_152641.4:c.4447_4448insATTCTT MANE Select	NP_689854.2:p.Ile1483delinsAsnSerPhe
NM_001347839.2:c.4447_4448insATTCTT	NP_001334768.1:p.Ile1483delinsAsnSerPhe