Canonical Allele Identifier: CA525732

Gene: ATAD3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1517750G>A , CM000663.2:g.1517750G>A	GRCh38
NC_000001.10:g.1453130G>A , CM000663.1:g.1453130G>A	GRCh37
NC_000001.9:g.1442993G>A	NCBI36
NG_053035.1:g.10608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339113.9:c.303G>A
ENST00000378756.8:c.419G>A MANE Select	ENSP00000368031.3:p.Arg140His
ENST00000536055.6:c.182G>A	ENSP00000439290.1:p.Arg61His
ENST00000672388.1:n.826G>A
ENST00000339113.8:c.375G>A
ENST00000378755.9:c.563G>A	ENSP00000368030.5:p.Arg188His
ENST00000378756.7:c.419G>A	ENSP00000368031.3:p.Arg140His
ENST00000429957.1:n.130G>A
ENST00000439513.1:n.378G>A
ENST00000536055.5:c.182G>A	ENSP00000439290.1:p.Arg61His
NM_001170535.1:c.419G>A	NP_001164006.1:p.Arg140His
NM_001170536.1:c.182G>A	NP_001164007.1:p.Arg61His
NM_018188.3:c.563G>A	NP_060658.3:p.Arg188His
NM_001170535.2:c.419G>A	NP_001164006.1:p.Arg140His
NM_001170536.2:c.182G>A	NP_001164007.1:p.Arg61His
NM_018188.4:c.563G>A	NP_060658.3:p.Arg188His
XM_024448098.1:c.419G>A	XP_024303866.1:p.Arg140His
XR_001737282.1:n.545G>A
XR_002956997.1:n.545G>A
NM_001170535.3:c.419G>A MANE Select	NP_001164006.1:p.Arg140His
NM_018188.5:c.563G>A	NP_060658.3:p.Arg188His
NM_001170536.3:c.182G>A	NP_001164007.1:p.Arg61His