Canonical Allele Identifier: CA2642610446

Gene: ATAD3A

Linked Data

• gnomAD v4: 1-1512435-AGCGCGCCGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512436_1512444del , CM000663.2:g.1512436_1512444del	GRCh38
NC_000001.10:g.1447816_1447824del , CM000663.1:g.1447816_1447824del	GRCh37
NC_000001.9:g.1437679_1437687del	NCBI36
NG_053035.1:g.5294_5302del

Transcript Alleles

HGVS	Amino-acid change
ENST00000339113.9:c.52_60del
ENST00000378756.8:c.168_176del MANE Select	ENSP00000368031.3:p.Glu56_Ala59delinsAsp
ENST00000672388.1:n.272_280del
ENST00000378755.9:c.168_176del	ENSP00000368030.5:p.Glu56_Ala59delinsAsp
ENST00000378756.7:c.168_176del	ENSP00000368031.3:p.Glu56_Ala59delinsAsp
NM_001170535.1:c.168_176del	NP_001164006.1:p.Glu56_Ala59delinsAsp
NM_018188.3:c.168_176del	NP_060658.3:p.Glu56_Ala59delinsAsp
NM_001170535.2:c.168_176del	NP_001164006.1:p.Glu56_Ala59delinsAsp
NM_018188.4:c.168_176del	NP_060658.3:p.Glu56_Ala59delinsAsp
XM_024448098.1:c.168_176del	XP_024303866.1:p.Glu56_Ala59delinsAsp
XR_001737282.1:n.294_302del
XR_002956997.1:n.294_302del
NM_001170535.3:c.168_176del MANE Select	NP_001164006.1:p.Glu56_Ala59delinsAsp
NM_018188.5:c.168_176del	NP_060658.3:p.Glu56_Ala59delinsAsp