Canonical Allele Identifier: CA525698

Gene: ATAD3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1517412C>T , CM000663.2:g.1517412C>T	GRCh38
NC_000001.10:g.1452792C>T , CM000663.1:g.1452792C>T	GRCh37
NC_000001.9:g.1442655C>T	NCBI36
NG_053035.1:g.10270C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339113.9:c.268C>T
ENST00000378756.8:c.384C>T MANE Select	ENSP00000368031.3:p.Ala128=
ENST00000536055.6:c.147C>T	ENSP00000439290.1:p.Ala49=
ENST00000672388.1:n.488C>T
ENST00000339113.8:c.340C>T
ENST00000378755.9:c.528C>T	ENSP00000368030.5:p.Ala176=
ENST00000378756.7:c.384C>T	ENSP00000368031.3:p.Ala128=
ENST00000439513.1:n.343C>T
ENST00000536055.5:c.147C>T	ENSP00000439290.1:p.Ala49=
NM_001170535.1:c.384C>T	NP_001164006.1:p.Ala128=
NM_001170536.1:c.147C>T	NP_001164007.1:p.Ala49=
NM_018188.3:c.528C>T	NP_060658.3:p.Ala176=
NM_001170535.2:c.384C>T	NP_001164006.1:p.Ala128=
NM_001170536.2:c.147C>T	NP_001164007.1:p.Ala49=
NM_018188.4:c.528C>T	NP_060658.3:p.Ala176=
XM_024448098.1:c.384C>T	XP_024303866.1:p.Ala128=
XR_001737282.1:n.510C>T
XR_002956997.1:n.510C>T
NM_001170535.3:c.384C>T MANE Select	NP_001164006.1:p.Ala128=
NM_018188.5:c.528C>T	NP_060658.3:p.Ala176=
NM_001170536.3:c.147C>T	NP_001164007.1:p.Ala49=