Canonical Allele Identifier: CA337845035

Gene: ATAD3A

Linked Data

• MyVariant Identifiers: chr1:g.1447662T>G (hg19) ; chr1:g.1512282T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512282T>G , CM000663.2:g.1512282T>G	GRCh38
NC_000001.10:g.1447662T>G , CM000663.1:g.1447662T>G	GRCh37
NC_000001.9:g.1437525T>G	NCBI36
NG_053035.1:g.5140T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378756.8:c.14T>G MANE Select	ENSP00000368031.3:p.Phe5Cys
ENST00000672388.1:n.118T>G
ENST00000378755.9:c.14T>G	ENSP00000368030.5:p.Phe5Cys
ENST00000378756.7:c.14T>G	ENSP00000368031.3:p.Phe5Cys
NM_001170535.1:c.14T>G	NP_001164006.1:p.Phe5Cys
NM_018188.3:c.14T>G	NP_060658.3:p.Phe5Cys
NM_001170535.2:c.14T>G	NP_001164006.1:p.Phe5Cys
NM_018188.4:c.14T>G	NP_060658.3:p.Phe5Cys
XM_024448098.1:c.14T>G	XP_024303866.1:p.Phe5Cys
XR_001737282.1:n.140T>G
XR_002956997.1:n.140T>G
NM_001170535.3:c.14T>G MANE Select	NP_001164006.1:p.Phe5Cys
NM_018188.5:c.14T>G	NP_060658.3:p.Phe5Cys