Canonical Allele Identifier: CA521010273

Gene: ATAD3A

Linked Data

• dbSNP Id: rs1295983741
• gnomAD v2: 1-1447722-CGCAGCCCGG-C
• gnomAD v3: 1-1512342-CGCAGCCCGG-C
• gnomAD v4: 1-1512342-CGCAGCCCGG-C
• MyVariant Identifiers: chr1:g.1447723_1447731del (hg19) ; chr1:g.1512343_1512351del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512344_1512352del , CM000663.2:g.1512344_1512352del	GRCh38
NC_000001.10:g.1447724_1447732del , CM000663.1:g.1447724_1447732del	GRCh37
NC_000001.9:g.1437587_1437595del	NCBI36
NG_053035.1:g.5202_5210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378756.8:c.76_84del MANE Select	ENSP00000368031.3:p.Gln26_Gly28del
ENST00000672388.1:n.180_188del
ENST00000378755.9:c.76_84del	ENSP00000368030.5:p.Gln26_Gly28del
ENST00000378756.7:c.76_84del	ENSP00000368031.3:p.Gln26_Gly28del
NM_001170535.1:c.76_84del	NP_001164006.1:p.Gln26_Gly28del
NM_018188.3:c.76_84del	NP_060658.3:p.Gln26_Gly28del
NM_001170535.2:c.76_84del	NP_001164006.1:p.Gln26_Gly28del
NM_018188.4:c.76_84del	NP_060658.3:p.Gln26_Gly28del
XM_024448098.1:c.76_84del	XP_024303866.1:p.Gln26_Gly28del
XR_001737282.1:n.202_210del
XR_002956997.1:n.202_210del
NM_001170535.3:c.76_84del MANE Select	NP_001164006.1:p.Gln26_Gly28del
NM_018188.5:c.76_84del	NP_060658.3:p.Gln26_Gly28del