Canonical Allele Identifier: CA604811920

Gene: ARID2

Linked Data

• dbSNP Id: rs1323262000
• gnomAD v2: 12-46246351-A-AG
• MyVariant Identifiers: chr12:g.46246351_46246352insG (hg19) ; chr12:g.45852568_45852569insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852568_45852569insG , CM000674.2:g.45852568_45852569insG	GRCh38
NC_000012.11:g.46246351_46246352insG , CM000674.1:g.46246351_46246352insG	GRCh37
NC_000012.10:g.44532618_44532619insG	NCBI36
NG_052800.1:g.127904_127905insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4445_4446insG	ENSP00000415650.3:p.Ile1483AsnfsTer20
ENST00000457135.2:c.654_655insG
ENST00000334344.11:c.4445_4446insG MANE Select	ENSP00000335044.6:p.Ile1483AsnfsTer20
ENST00000422737.6:c.4366_4367insG
ENST00000334344.10:c.4445_4446insG	ENSP00000335044.6:p.Ile1483AsnfsTer20
ENST00000422737.5:c.3998_3999insG	ENSP00000415650.1:p.Ile1334AsnfsTer20
ENST00000444670.5:c.3275_3276insG	ENSP00000397307.1:p.Ile1093AsnfsTer20
ENST00000457135.1:c.269_270insG	ENSP00000388357.1:p.Ile91AsnfsTer20
ENST00000479608.5:n.3736_3737insG
NM_152641.2:c.4445_4446insG	NP_689854.2:p.Ile1483AsnfsTer20
XM_006719272.2:c.4445_4446insG	XP_006719335.1:p.Ile1483AsnfsTer20
XM_011538025.1:c.2813_2814insG	XP_011536327.1:p.Ile939AsnfsTer20
XR_944505.1:n.4593_4594insG
NM_001347839.1:c.4445_4446insG	NP_001334768.1:p.Ile1483AsnfsTer20
NM_152641.3:c.4445_4446insG	NP_689854.2:p.Ile1483AsnfsTer20
XM_006719272.4:c.4445_4446insG	XP_006719335.1:p.Ile1483AsnfsTer20
XR_944505.3:n.4576_4577insG
NM_152641.4:c.4445_4446insG MANE Select	NP_689854.2:p.Ile1483AsnfsTer20
NM_001347839.2:c.4445_4446insG	NP_001334768.1:p.Ile1483AsnfsTer20