Canonical Allele Identifier: CA525984

Gene: ATAD3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1522785C>T , CM000663.2:g.1522785C>T	GRCh38
NC_000001.10:g.1458165C>T , CM000663.1:g.1458165C>T	GRCh37
NC_000001.9:g.1448028C>T	NCBI36
NG_053035.1:g.15643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339113.9:c.756C>T
ENST00000378756.8:c.792C>T MANE Select	ENSP00000368031.3:p.Ala264=
ENST00000536055.6:c.555C>T	ENSP00000439290.1:p.Ala185=
ENST00000672388.1:n.1129C>T
ENST00000339113.8:c.748C>T
ENST00000378755.9:c.936C>T	ENSP00000368030.5:p.Ala312=
ENST00000378756.7:c.792C>T	ENSP00000368031.3:p.Ala264=
ENST00000536055.5:c.555C>T	ENSP00000439290.1:p.Ala185=
NM_001170535.1:c.792C>T	NP_001164006.1:p.Ala264=
NM_001170536.1:c.555C>T	NP_001164007.1:p.Ala185=
NM_018188.3:c.936C>T	NP_060658.3:p.Ala312=
NM_001170535.2:c.792C>T	NP_001164006.1:p.Ala264=
NM_001170536.2:c.555C>T	NP_001164007.1:p.Ala185=
NM_018188.4:c.936C>T	NP_060658.3:p.Ala312=
XM_024448098.1:c.792C>T	XP_024303866.1:p.Ala264=
XR_001737282.1:n.918C>T
XR_002956997.1:n.918C>T
NM_001170535.3:c.792C>T MANE Select	NP_001164006.1:p.Ala264=
NM_018188.5:c.936C>T	NP_060658.3:p.Ala312=
NM_001170536.3:c.555C>T	NP_001164007.1:p.Ala185=