Canonical Allele Identifier: CA604811921

Gene: ARID2

Linked Data

• dbSNP Id: rs1201460869
• gnomAD v2: 12-46246352-A-AAATTCTTTCTAGTTG
• MyVariant Identifiers: chr12:g.46246352_46246353insAATTCTTTCTAGTTG (hg19) ; chr12:g.45852569_45852570insAATTCTTTCTAGTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852570_45852571insATTCTTTCTAGTTGA , CM000674.2:g.45852570_45852571insATTCTTTCTAGTTGA	GRCh38
NC_000012.11:g.46246353_46246354insATTCTTTCTAGTTGA , CM000674.1:g.46246353_46246354insATTCTTTCTAGTTGA	GRCh37
NC_000012.10:g.44532620_44532621insATTCTTTCTAGTTGA	NCBI36
NG_052800.1:g.127906_127907insATTCTTTCTAGTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4447_4448insATTCTTTCTAGTTGA	ENSP00000415650.3:p.Ile1483AsnfsTer4
ENST00000457135.2:c.656_657insATTCTTTCTAGTTGA
ENST00000334344.11:c.4447_4448insATTCTTTCTAGTTGA MANE Select	ENSP00000335044.6:p.Ile1483AsnfsTer4
ENST00000422737.6:c.4368_4369insATTCTTTCTAGTTGA
ENST00000334344.10:c.4447_4448insATTCTTTCTAGTTGA	ENSP00000335044.6:p.Ile1483AsnfsTer4
ENST00000422737.5:c.4000_4001insATTCTTTCTAGTTGA	ENSP00000415650.1:p.Ile1334AsnfsTer4
ENST00000444670.5:c.3277_3278insATTCTTTCTAGTTGA	ENSP00000397307.1:p.Ile1093AsnfsTer4
ENST00000457135.1:c.271_272insATTCTTTCTAGTTGA	ENSP00000388357.1:p.Ile91AsnfsTer4
ENST00000479608.5:n.3738_3739insATTCTTTCTAGTTGA
NM_152641.2:c.4447_4448insATTCTTTCTAGTTGA	NP_689854.2:p.Ile1483AsnfsTer4
XM_006719272.2:c.4447_4448insATTCTTTCTAGTTGA	XP_006719335.1:p.Ile1483AsnfsTer4
XM_011538025.1:c.2815_2816insATTCTTTCTAGTTGA	XP_011536327.1:p.Ile939AsnfsTer4
XR_944505.1:n.4595_4596insATTCTTTCTAGTTGA
NM_001347839.1:c.4447_4448insATTCTTTCTAGTTGA	NP_001334768.1:p.Ile1483AsnfsTer4
NM_152641.3:c.4447_4448insATTCTTTCTAGTTGA	NP_689854.2:p.Ile1483AsnfsTer4
XM_006719272.4:c.4447_4448insATTCTTTCTAGTTGA	XP_006719335.1:p.Ile1483AsnfsTer4
XR_944505.3:n.4578_4579insATTCTTTCTAGTTGA
NM_152641.4:c.4447_4448insATTCTTTCTAGTTGA MANE Select	NP_689854.2:p.Ile1483AsnfsTer4
NM_001347839.2:c.4447_4448insATTCTTTCTAGTTGA	NP_001334768.1:p.Ile1483AsnfsTer4