Canonical Allele Identifier: CA415385392

Gene: ATAD3A

Linked Data

• MyVariant Identifiers: chr1:g.1447822C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512442C>G , CM000663.2:g.1512442C>G	GRCh38
NC_000001.10:g.1447822C>G , CM000663.1:g.1447822C>G	GRCh37
NC_000001.9:g.1437685C>G	NCBI36
NG_053035.1:g.5300C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000339113.9:c.58C>G
ENST00000378756.8:c.174C>G MANE Select	ENSP00000368031.3:p.Ala58=
ENST00000672388.1:n.278C>G
ENST00000378755.9:c.174C>G	ENSP00000368030.5:p.Ala58=
ENST00000378756.7:c.174C>G	ENSP00000368031.3:p.Ala58=
NM_001170535.1:c.174C>G	NP_001164006.1:p.Ala58=
NM_018188.3:c.174C>G	NP_060658.3:p.Ala58=
NM_001170535.2:c.174C>G	NP_001164006.1:p.Ala58=
NM_018188.4:c.174C>G	NP_060658.3:p.Ala58=
XM_024448098.1:c.174C>G	XP_024303866.1:p.Ala58=
XR_001737282.1:n.300C>G
XR_002956997.1:n.300C>G
NM_001170535.3:c.174C>G MANE Select	NP_001164006.1:p.Ala58=
NM_018188.5:c.174C>G	NP_060658.3:p.Ala58=