Canonical Allele Identifier: CA16040615
Gene: ATAD3A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225697
dbSNP Id: rs1057517687

User contributed link-outs

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000378755.9:c.158C>T ENSP00000368030.5:p.Thr53Ile
ENST00000378756.7:c.158C>T ENSP00000368031.3:p.Thr53Ile
NM_001170535.1:c.158C>T VV NP_001164006.1:p.Thr53Ile
NM_018188.3:c.158C>T VV NP_060658.3:p.Thr53Ile