Canonical Allele Identifier: CA525849

Gene: ATAD3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1520197G>A , CM000663.2:g.1520197G>A	GRCh38
NC_000001.10:g.1455577G>A , CM000663.1:g.1455577G>A	GRCh37
NC_000001.9:g.1445440G>A	NCBI36
NG_053035.1:g.13055G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339113.9:c.535G>A
ENST00000378756.8:c.571G>A MANE Select	ENSP00000368031.3:p.Ala191Thr
ENST00000536055.6:c.334G>A	ENSP00000439290.1:p.Ala112Thr
ENST00000672388.1:n.978G>A
ENST00000339113.8:c.527G>A
ENST00000378755.9:c.715G>A	ENSP00000368030.5:p.Ala239Thr
ENST00000378756.7:c.571G>A	ENSP00000368031.3:p.Ala191Thr
ENST00000429957.1:n.282G>A
ENST00000536055.5:c.334G>A	ENSP00000439290.1:p.Ala112Thr
NM_001170535.1:c.571G>A	NP_001164006.1:p.Ala191Thr
NM_001170536.1:c.334G>A	NP_001164007.1:p.Ala112Thr
NM_018188.3:c.715G>A	NP_060658.3:p.Ala239Thr
NM_001170535.2:c.571G>A	NP_001164006.1:p.Ala191Thr
NM_001170536.2:c.334G>A	NP_001164007.1:p.Ala112Thr
NM_018188.4:c.715G>A	NP_060658.3:p.Ala239Thr
XM_024448098.1:c.571G>A	XP_024303866.1:p.Ala191Thr
XR_001737282.1:n.697G>A
XR_002956997.1:n.697G>A
NM_001170535.3:c.571G>A MANE Select	NP_001164006.1:p.Ala191Thr
NM_018188.5:c.715G>A	NP_060658.3:p.Ala239Thr
NM_001170536.3:c.334G>A	NP_001164007.1:p.Ala112Thr