Canonical Allele Identifier: CA889543184

Gene: GATAD2B

Linked Data

• dbSNP Id: rs1457800011
• gnomAD v3: 1-153819710-G-GT
• gnomAD v4: 1-153819710-G-GT
• MyVariant Identifiers: chr1:g.153792186_153792187insT (hg19) ; chr1:g.153819710_153819711insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819710_153819711insT , CM000663.2:g.153819710_153819711insT	GRCh38
NC_000001.10:g.153792186_153792187insT , CM000663.1:g.153792186_153792187insT	GRCh37
NC_000001.9:g.152058810_152058811insT	NCBI36
NG_050988.1:g.108265_108266insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.-64_-63insA	ENSP00000515408.1:n.-64_-63insA
ENST00000368655.5:c.360_361insA MANE Select	ENSP00000357644.4:p.Pro121ThrfsTer10
ENST00000638051.1:n.78_79insA
ENST00000368655.4:c.360_361insA	ENSP00000357644.4:p.Pro121ThrfsTer10
ENST00000634401.1:c.360_361insA	ENSP00000489313.1:p.Pro121ThrfsTer10
ENST00000634408.1:c.360_361insA	ENSP00000489595.1:p.Pro121ThrfsTer10
ENST00000634544.1:c.360_361insA	ENSP00000489184.1:p.Pro121ThrfsTer10
ENST00000634791.1:c.360_361insA	ENSP00000489566.1:p.Pro121ThrfsTer10
NM_020699.2:c.360_361insA	NP_065750.1:p.Pro121ThrfsTer10
XM_005245364.3:c.360_361insA	XP_005245421.1:p.Pro121ThrfsTer10
XM_006711469.2:c.360_361insA	XP_006711532.1:p.Pro121ThrfsTer10
XM_011509808.1:c.360_361insA	XP_011508110.1:p.Pro121ThrfsTer10
NM_020699.3:c.360_361insA	NP_065750.1:p.Pro121ThrfsTer10
XM_005245364.4:c.360_361insA	XP_005245421.1:p.Pro121ThrfsTer10
XM_024448621.1:c.360_361insA	XP_024304389.1:p.Pro121ThrfsTer10
NM_020699.4:c.360_361insA MANE Select	NP_065750.1:p.Pro121ThrfsTer10