Canonical Allele Identifier: CA2642610099
Gene: ATAD3A HGNC NCBI

Linked Data

gnomAD v4: 1-1512231-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512231G>A , CM000663.2:g.1512231G>A GRCh38
NC_000001.10:g.1447611G>A , CM000663.1:g.1447611G>A GRCh37
NC_000001.9:g.1437474G>A NCBI36
NG_053035.1:g.5089G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.-38G>A MANE Select ENSP00000368031.3:n.-38G>A
ENST00000672388.1:n.67G>A
ENST00000378755.9:c.-38G>A ENSP00000368030.5:n.-38G>A
ENST00000378756.7:c.-38G>A ENSP00000368031.3:n.-38G>A
NM_001170535.1:c.-38G>A NP_001164006.1:n.-38G>A
NM_018188.3:c.-38G>A NP_060658.3:n.-38G>A
NM_001170535.2:c.-38G>A NP_001164006.1:n.-38G>A
NM_018188.4:c.-38G>A NP_060658.3:n.-38G>A
XM_024448098.1:c.-38G>A XP_024303866.1:n.-38G>A
XR_001737282.1:n.89G>A
XR_002956997.1:n.89G>A
NM_001170535.3:c.-38G>A MANE Select NP_001164006.1:n.-38G>A
NM_018188.5:c.-38G>A NP_060658.3:n.-38G>A