Canonical Allele Identifier: CA1149097920
Gene: ATAD3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512433G= , CM000663.2:g.1512433G= GRCh38
NC_000001.10:g.1447813G= , CM000663.1:g.1447813G= GRCh37
NC_000001.9:g.1437676G= NCBI36
NG_053035.1:g.5291G=

Transcript Alleles

HGVS Amino-acid change
ENST00000339113.9:c.49G=
ENST00000378756.8:c.165G= MANE Select ENSP00000368031.3:p.Leu55=
ENST00000672388.1:n.269G=
ENST00000378755.9:c.165G= ENSP00000368030.5:p.Leu55=
ENST00000378756.7:c.165G= ENSP00000368031.3:p.Leu55=
NM_001170535.1:c.165G= NP_001164006.1:p.Leu55=
NM_018188.3:c.165G= NP_060658.3:p.Leu55=
NM_001170535.2:c.165G= NP_001164006.1:p.Leu55=
NM_018188.4:c.165G= NP_060658.3:p.Leu55=
XM_024448098.1:c.165G= XP_024303866.1:p.Leu55=
XR_001737282.1:n.291G=
XR_002956997.1:n.291G=
NM_001170535.3:c.165G= MANE Select NP_001164006.1:p.Leu55=
NM_018188.5:c.165G= NP_060658.3:p.Leu55=