Canonical Allele Identifier: CA1149097917
Community Standard Title: NM_001170535.3(ATAD3A):c.158C= (p.Thr53=)
Gene: ATAD3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512426C= , CM000663.2:g.1512426C= GRCh38
NC_000001.10:g.1447806C= , CM000663.1:g.1447806C= GRCh37
NC_000001.9:g.1437669C= NCBI36
NG_053035.1:g.5284C=

Transcript Alleles

HGVS Amino-acid Change
NM_001170535.3:c.158C= MANE Select NP_001164006.1:p.Thr53=
ENST00000378756.8:c.158C= MANE Select ENSP00000368031.3:p.Thr53=
NM_001170535.1:c.158C= NP_001164006.1:p.Thr53=
NM_001170535.2:c.158C= NP_001164006.1:p.Thr53=
NM_018188.3:c.158C= NP_060658.3:p.Thr53=
NM_018188.4:c.158C= NP_060658.3:p.Thr53=
NM_018188.5:c.158C= NP_060658.3:p.Thr53=
ENST00000339113.9:c.42C=
ENST00000378755.9:c.158C= ENSP00000368030.5:p.Thr53=
ENST00000378756.7:c.158C= ENSP00000368031.3:p.Thr53=
ENST00000672388.1:n.262C=
XM_024448098.1:c.158C= XP_024303866.1:p.Thr53=
XR_001737282.1:n.284C=
XR_002956997.1:n.284C=