Canonical Allele Identifier: CA2648088524
Gene: GATAD2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153811973_153811983del , CM000663.2:g.153811973_153811983del GRCh38
NC_000001.10:g.153784449_153784459del , CM000663.1:g.153784449_153784459del GRCh37
NC_000001.9:g.152051073_152051083del NCBI36
NG_050988.1:g.116001_116011del

Transcript Alleles

HGVS Amino-acid change
ENST00000368655.5:c.1530+47_1530+57del MANE Select ENSP00000357644.4:n.1530+47_1530+57del
ENST00000637918.1:c.17+47_17+57del
ENST00000368655.4:c.1530+47_1530+57del ENSP00000357644.4:n.1530+47_1530+57del
ENST00000634408.1:c.1482+47_1482+57del ENSP00000489595.1:n.1482+47_1482+57del
ENST00000634544.1:c.1530+47_1530+57del ENSP00000489184.1:n.1530+47_1530+57del
ENST00000634564.1:c.784+47_784+57del
ENST00000634645.1:n.254+47_254+57del
NM_020699.2:c.1530+47_1530+57del NP_065750.1:n.1530+47_1530+57del
XM_005245364.3:c.1530+47_1530+57del XP_005245421.1:n.1530+47_1530+57del
XM_006711469.2:c.1530+47_1530+57del XP_006711532.1:n.1530+47_1530+57del
XM_011509808.1:c.1530+47_1530+57del XP_011508110.1:n.1530+47_1530+57del
NM_020699.3:c.1530+47_1530+57del NP_065750.1:n.1530+47_1530+57del
XM_005245364.4:c.1530+47_1530+57del XP_005245421.1:n.1530+47_1530+57del
XM_024448621.1:c.1530+47_1530+57del XP_024304389.1:n.1530+47_1530+57del
NM_020699.4:c.1530+47_1530+57del MANE Select NP_065750.1:n.1530+47_1530+57del