Canonical Allele Identifier: CA645532344

Gene: GATAD2B

Linked Data

• COSMIC: COSM1688649

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819709_153819710delinsAA , CM000663.2:g.153819709_153819710delinsAA	GRCh38
NC_000001.10:g.153792185_153792186delinsAA , CM000663.1:g.153792185_153792186delinsAA	GRCh37
NC_000001.9:g.152058809_152058810delinsAA	NCBI36
NG_050988.1:g.108266_108267delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.-63_-62delinsTT	ENSP00000515408.1:n.-63_-62delinsTT
ENST00000368655.5:c.361_362delinsTT MANE Select	ENSP00000357644.4:p.Pro121Phe
ENST00000638051.1:n.79_80delinsTT
ENST00000368655.4:c.361_362delinsTT	ENSP00000357644.4:p.Pro121Phe
ENST00000634401.1:c.361_362delinsTT	ENSP00000489313.1:p.Pro121Phe
ENST00000634408.1:c.361_362delinsTT	ENSP00000489595.1:p.Pro121Phe
ENST00000634544.1:c.361_362delinsTT	ENSP00000489184.1:p.Pro121Phe
ENST00000634791.1:c.361_362delinsTT	ENSP00000489566.1:p.Pro121Phe
NM_020699.2:c.361_362delinsTT	NP_065750.1:p.Pro121Phe
XM_005245364.3:c.361_362delinsTT	XP_005245421.1:p.Pro121Phe
XM_006711469.2:c.361_362delinsTT	XP_006711532.1:p.Pro121Phe
XM_011509808.1:c.361_362delinsTT	XP_011508110.1:p.Pro121Phe
NM_020699.3:c.361_362delinsTT	NP_065750.1:p.Pro121Phe
XM_005245364.4:c.361_362delinsTT	XP_005245421.1:p.Pro121Phe
XM_024448621.1:c.361_362delinsTT	XP_024304389.1:p.Pro121Phe
NM_020699.4:c.361_362delinsTT MANE Select	NP_065750.1:p.Pro121Phe