Canonical Allele Identifier: CA2506502919

Gene: GATAD2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819689_153819690insCTTAG , CM000663.2:g.153819689_153819690insCTTAG	GRCh38
NC_000001.10:g.153792165_153792166insCTTAG , CM000663.1:g.153792165_153792166insCTTAG	GRCh37
NC_000001.9:g.152058789_152058790insCTTAG	NCBI36
NG_050988.1:g.108286_108287insCTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.-43_-42insCTAAG	ENSP00000515408.1:n.-43_-42insCTAAG
ENST00000368655.5:c.381_382insCTAAG MANE Select	ENSP00000357644.4:p.Asp130CysfsTer24
ENST00000638051.1:n.99_100insCTAAG
ENST00000368655.4:c.381_382insCTAAG	ENSP00000357644.4:p.Asp130CysfsTer24
ENST00000634401.1:c.381_382insCTAAG	ENSP00000489313.1:p.Asp130CysfsTer24
ENST00000634408.1:c.381_382insCTAAG	ENSP00000489595.1:p.Asp130CysfsTer24
ENST00000634544.1:c.381_382insCTAAG	ENSP00000489184.1:p.Asp130CysfsTer24
ENST00000634791.1:c.381_382insCTAAG	ENSP00000489566.1:p.Asp130CysfsTer?
NM_020699.2:c.381_382insCTAAG	NP_065750.1:p.Asp130CysfsTer24
XM_005245364.3:c.381_382insCTAAG	XP_005245421.1:p.Asp130CysfsTer24
XM_006711469.2:c.381_382insCTAAG	XP_006711532.1:p.Asp130CysfsTer24
XM_011509808.1:c.381_382insCTAAG	XP_011508110.1:p.Asp130CysfsTer24
NM_020699.3:c.381_382insCTAAG	NP_065750.1:p.Asp130CysfsTer24
XM_005245364.4:c.381_382insCTAAG	XP_005245421.1:p.Asp130CysfsTer24
XM_024448621.1:c.381_382insCTAAG	XP_024304389.1:p.Asp130CysfsTer24
NM_020699.4:c.381_382insCTAAG MANE Select	NP_065750.1:p.Asp130CysfsTer24