Canonical Allele Identifier: CA337846522

Gene: ATAD3A

Linked Data

• MyVariant Identifiers: chr1:g.1447806C>G (hg19) ; chr1:g.1512426C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512426C>G , CM000663.2:g.1512426C>G	GRCh38
NC_000001.10:g.1447806C>G , CM000663.1:g.1447806C>G	GRCh37
NC_000001.9:g.1437669C>G	NCBI36
NG_053035.1:g.5284C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000339113.9:c.42C>G
ENST00000378756.8:c.158C>G MANE Select	ENSP00000368031.3:p.Thr53Ser
ENST00000672388.1:n.262C>G
ENST00000378755.9:c.158C>G	ENSP00000368030.5:p.Thr53Ser
ENST00000378756.7:c.158C>G	ENSP00000368031.3:p.Thr53Ser
NM_001170535.1:c.158C>G	NP_001164006.1:p.Thr53Ser
NM_018188.3:c.158C>G	NP_060658.3:p.Thr53Ser
NM_001170535.2:c.158C>G	NP_001164006.1:p.Thr53Ser
NM_018188.4:c.158C>G	NP_060658.3:p.Thr53Ser
XM_024448098.1:c.158C>G	XP_024303866.1:p.Thr53Ser
XR_001737282.1:n.284C>G
XR_002956997.1:n.284C>G
NM_001170535.3:c.158C>G MANE Select	NP_001164006.1:p.Thr53Ser
NM_018188.5:c.158C>G	NP_060658.3:p.Thr53Ser