Canonical Allele Identifier: CA415385288
Gene: ATAD3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1447669T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512289T>A , CM000663.2:g.1512289T>A GRCh38
NC_000001.10:g.1447669T>A , CM000663.1:g.1447669T>A GRCh37
NC_000001.9:g.1437532T>A NCBI36
NG_053035.1:g.5147T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.21T>A MANE Select ENSP00000368031.3:p.Ile7=
ENST00000672388.1:n.125T>A
ENST00000378755.9:c.21T>A ENSP00000368030.5:p.Ile7=
ENST00000378756.7:c.21T>A ENSP00000368031.3:p.Ile7=
NM_001170535.1:c.21T>A NP_001164006.1:p.Ile7=
NM_018188.3:c.21T>A NP_060658.3:p.Ile7=
NM_001170535.2:c.21T>A NP_001164006.1:p.Ile7=
NM_018188.4:c.21T>A NP_060658.3:p.Ile7=
XM_024448098.1:c.21T>A XP_024303866.1:p.Ile7=
XR_001737282.1:n.147T>A
XR_002956997.1:n.147T>A
NM_001170535.3:c.21T>A MANE Select NP_001164006.1:p.Ile7=
NM_018188.5:c.21T>A NP_060658.3:p.Ile7=