Canonical Allele Identifier: CA526369927

Gene: GATAD2B

Linked Data

• dbSNP Id: rs1303458801
• gnomAD v2: 1-153792070-CTT-C
• gnomAD v4: 1-153819594-CTT-C
• MyVariant Identifiers: chr1:g.153792071_153792072del (hg19) ; chr1:g.153819595_153819596del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819596_153819597del , CM000663.2:g.153819596_153819597del	GRCh38
NC_000001.10:g.153792072_153792073del , CM000663.1:g.153792072_153792073del	GRCh37
NC_000001.9:g.152058696_152058697del	NCBI36
NG_050988.1:g.108380_108381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.42+10_42+11del	ENSP00000515408.1:n.42+10_42+11del
ENST00000368655.5:c.465+10_465+11del MANE Select	ENSP00000357644.4:n.465+10_465+11del
ENST00000368655.4:c.465+10_465+11del	ENSP00000357644.4:n.465+10_465+11del
ENST00000634401.1:c.465+10_465+11del	ENSP00000489313.1:n.465+10_465+11del
ENST00000634408.1:c.465+10_465+11del	ENSP00000489595.1:n.465+10_465+11del
ENST00000634544.1:c.465+10_465+11del	ENSP00000489184.1:n.465+10_465+11del
NM_020699.2:c.465+10_465+11del	NP_065750.1:n.465+10_465+11del
XM_005245364.3:c.465+10_465+11del	XP_005245421.1:n.465+10_465+11del
XM_006711469.2:c.465+10_465+11del	XP_006711532.1:n.465+10_465+11del
XM_011509808.1:c.465+10_465+11del	XP_011508110.1:n.465+10_465+11del
NM_020699.3:c.465+10_465+11del	NP_065750.1:n.465+10_465+11del
XM_005245364.4:c.465+10_465+11del	XP_005245421.1:n.465+10_465+11del
XM_024448621.1:c.465+10_465+11del	XP_024304389.1:n.465+10_465+11del
NM_020699.4:c.465+10_465+11del MANE Select	NP_065750.1:n.465+10_465+11del