Canonical Allele Identifier: CA2648090604
Gene: GATAD2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819884_153819887del , CM000663.2:g.153819884_153819887del GRCh38
NC_000001.10:g.153792360_153792363del , CM000663.1:g.153792360_153792363del GRCh37
NC_000001.9:g.152058984_152058987del NCBI36
NG_050988.1:g.108089_108092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703630.1:c.-88-152_-88-149del ENSP00000515408.1:n.-88-152_-88-149del
ENST00000368655.5:c.336-152_336-149del MANE Select ENSP00000357644.4:n.336-152_336-149del
ENST00000638051.1:n.54-152_54-149del
ENST00000368655.4:c.336-152_336-149del ENSP00000357644.4:n.336-152_336-149del
ENST00000634401.1:c.336-152_336-149del ENSP00000489313.1:n.336-152_336-149del
ENST00000634408.1:c.336-152_336-149del ENSP00000489595.1:n.336-152_336-149del
ENST00000634544.1:c.336-152_336-149del ENSP00000489184.1:n.336-152_336-149del
ENST00000634791.1:c.336-152_336-149del ENSP00000489566.1:n.336-152_336-149del
NM_020699.2:c.336-152_336-149del NP_065750.1:n.336-152_336-149del
XM_005245364.3:c.336-152_336-149del XP_005245421.1:n.336-152_336-149del
XM_006711469.2:c.336-152_336-149del XP_006711532.1:n.336-152_336-149del
XM_011509808.1:c.336-152_336-149del XP_011508110.1:n.336-152_336-149del
NM_020699.3:c.336-152_336-149del NP_065750.1:n.336-152_336-149del
XM_005245364.4:c.336-152_336-149del XP_005245421.1:n.336-152_336-149del
XM_024448621.1:c.336-152_336-149del XP_024304389.1:n.336-152_336-149del
NM_020699.4:c.336-152_336-149del MANE Select NP_065750.1:n.336-152_336-149del