Canonical Allele Identifier: CA2642610455

Gene: ATAD3A

Linked Data

• gnomAD v4: 1-1512438-GCGCCGCCAAGGCGGCGCGCGAGCTGGAGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512440_1512469del , CM000663.2:g.1512440_1512469del	GRCh38
NC_000001.10:g.1447820_1447849del , CM000663.1:g.1447820_1447849del	GRCh37
NC_000001.9:g.1437683_1437712del	NCBI36
NG_053035.1:g.5298_5327del

Transcript Alleles

HGVS	Amino-acid change
ENST00000339113.9:c.56_85del
ENST00000378756.8:c.172_201del MANE Select	ENSP00000368031.3:p.Ala58_His67del
ENST00000672388.1:n.276_305del
ENST00000378755.9:c.172_201del	ENSP00000368030.5:p.Ala58_His67del
ENST00000378756.7:c.172_201del	ENSP00000368031.3:p.Ala58_His67del
NM_001170535.1:c.172_201del	NP_001164006.1:p.Ala58_His67del
NM_018188.3:c.172_201del	NP_060658.3:p.Ala58_His67del
NM_001170535.2:c.172_201del	NP_001164006.1:p.Ala58_His67del
NM_018188.4:c.172_201del	NP_060658.3:p.Ala58_His67del
XM_024448098.1:c.172_201del	XP_024303866.1:p.Ala58_His67del
XR_001737282.1:n.298_327del
XR_002956997.1:n.298_327del
NM_001170535.3:c.172_201del MANE Select	NP_001164006.1:p.Ala58_His67del
NM_018188.5:c.172_201del	NP_060658.3:p.Ala58_His67del