Canonical Allele Identifier: CA526554
Gene: ATAD3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1534014A>T , CM000663.2:g.1534014A>T GRCh38
NC_000001.10:g.1469394A>T , CM000663.1:g.1469394A>T GRCh37
NC_000001.9:g.1459257A>T NCBI36
NG_041807.1:g.11347T>A
NG_053035.1:g.26872A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339113.9:c.1667A>T
ENST00000378756.8:c.1703A>T MANE Select ENSP00000368031.3:p.Lys568Met
ENST00000400830.4:c.702A>T
ENST00000536055.6:c.1466A>T ENSP00000439290.1:p.Lys489Met
ENST00000672388.1:n.2040A>T
ENST00000339113.8:c.1659A>T
ENST00000378755.9:c.1847A>T ENSP00000368030.5:p.Lys616Met
ENST00000378756.7:c.1703A>T ENSP00000368031.3:p.Lys568Met
ENST00000536055.5:c.1466A>T ENSP00000439290.1:p.Lys489Met
NM_001170535.1:c.1703A>T NP_001164006.1:p.Lys568Met
NM_001170536.1:c.1466A>T NP_001164007.1:p.Lys489Met
NM_018188.3:c.1847A>T NP_060658.3:p.Lys616Met
NM_001170535.2:c.1703A>T NP_001164006.1:p.Lys568Met
NM_001170536.2:c.1466A>T NP_001164007.1:p.Lys489Met
NM_018188.4:c.1847A>T NP_060658.3:p.Lys616Met
XM_024448098.1:c.1781A>T XP_024303866.1:p.Lys594Met
XR_001737282.1:n.1776A>T
XR_002956997.1:n.1854A>T
NM_001170535.3:c.1703A>T MANE Select NP_001164006.1:p.Lys568Met
NM_018188.5:c.1847A>T NP_060658.3:p.Lys616Met
NM_001170536.3:c.1466A>T NP_001164007.1:p.Lys489Met