Canonical Allele Identifier: CA1149097882
Gene: ATAD3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512336C= , CM000663.2:g.1512336C= GRCh38
NC_000001.10:g.1447716C= , CM000663.1:g.1447716C= GRCh37
NC_000001.9:g.1437579C= NCBI36
NG_053035.1:g.5194C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.68C= MANE Select ENSP00000368031.3:p.Pro23=
ENST00000672388.1:n.172C=
ENST00000378755.9:c.68C= ENSP00000368030.5:p.Pro23=
ENST00000378756.7:c.68C= ENSP00000368031.3:p.Pro23=
NM_001170535.1:c.68C= NP_001164006.1:p.Pro23=
NM_018188.3:c.68C= NP_060658.3:p.Pro23=
NM_001170535.2:c.68C= NP_001164006.1:p.Pro23=
NM_018188.4:c.68C= NP_060658.3:p.Pro23=
XM_024448098.1:c.68C= XP_024303866.1:p.Pro23=
XR_001737282.1:n.194C=
XR_002956997.1:n.194C=
NM_001170535.3:c.68C= MANE Select NP_001164006.1:p.Pro23=
NM_018188.5:c.68C= NP_060658.3:p.Pro23=