Canonical Allele Identifier: CA415385286
Gene: ATAD3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1447666C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512286C>G , CM000663.2:g.1512286C>G GRCh38
NC_000001.10:g.1447666C>G , CM000663.1:g.1447666C>G GRCh37
NC_000001.9:g.1437529C>G NCBI36
NG_053035.1:g.5144C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.18C>G MANE Select ENSP00000368031.3:p.Gly6=
ENST00000672388.1:n.122C>G
ENST00000378755.9:c.18C>G ENSP00000368030.5:p.Gly6=
ENST00000378756.7:c.18C>G ENSP00000368031.3:p.Gly6=
NM_001170535.1:c.18C>G NP_001164006.1:p.Gly6=
NM_018188.3:c.18C>G NP_060658.3:p.Gly6=
NM_001170535.2:c.18C>G NP_001164006.1:p.Gly6=
NM_018188.4:c.18C>G NP_060658.3:p.Gly6=
XM_024448098.1:c.18C>G XP_024303866.1:p.Gly6=
XR_001737282.1:n.144C>G
XR_002956997.1:n.144C>G
NM_001170535.3:c.18C>G MANE Select NP_001164006.1:p.Gly6=
NM_018188.5:c.18C>G NP_060658.3:p.Gly6=