Canonical Allele Identifier: CA1149097822
Gene: ATAD3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512237C= , CM000663.2:g.1512237C= GRCh38
NC_000001.10:g.1447617C= , CM000663.1:g.1447617C= GRCh37
NC_000001.9:g.1437480C= NCBI36
NG_053035.1:g.5095C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378756.8:c.-32C= MANE Select ENSP00000368031.3:n.-32C=
ENST00000672388.1:n.73C=
ENST00000378755.9:c.-32C= ENSP00000368030.5:n.-32C=
ENST00000378756.7:c.-32C= ENSP00000368031.3:n.-32C=
NM_001170535.1:c.-32C= NP_001164006.1:n.-32C=
NM_018188.3:c.-32C= NP_060658.3:n.-32C=
NM_001170535.2:c.-32C= NP_001164006.1:n.-32C=
NM_018188.4:c.-32C= NP_060658.3:n.-32C=
XM_024448098.1:c.-32C= XP_024303866.1:n.-32C=
XR_001737282.1:n.95C=
XR_002956997.1:n.95C=
NM_001170535.3:c.-32C= MANE Select NP_001164006.1:n.-32C=
NM_018188.5:c.-32C= NP_060658.3:n.-32C=