Canonical Allele Identifier: CA1149097887
Gene: ATAD3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512342_1512351delinsCGCAGCCCGG , CM000663.2:g.1512342_1512351delinsCGCAGCCCGG GRCh38
NC_000001.10:g.1447722_1447731delinsCGCAGCCCGG , CM000663.1:g.1447722_1447731delinsCGCAGCCCGG GRCh37
NC_000001.9:g.1437585_1437594delinsCGCAGCCCGG NCBI36
NG_053035.1:g.5200_5209delinsCGCAGCCCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.74_83delinsCGCAGCCCGG MANE Select ENSP00000368031.3:p.Ala25=
ENST00000672388.1:n.178_187delinsCGCAGCCCGG
ENST00000378755.9:c.74_83delinsCGCAGCCCGG ENSP00000368030.5:p.Ala25=
ENST00000378756.7:c.74_83delinsCGCAGCCCGG ENSP00000368031.3:p.Ala25=
NM_001170535.1:c.74_83delinsCGCAGCCCGG NP_001164006.1:p.Ala25=
NM_018188.3:c.74_83delinsCGCAGCCCGG NP_060658.3:p.Ala25=
NM_001170535.2:c.74_83delinsCGCAGCCCGG NP_001164006.1:p.Ala25=
NM_018188.4:c.74_83delinsCGCAGCCCGG NP_060658.3:p.Ala25=
XM_024448098.1:c.74_83delinsCGCAGCCCGG XP_024303866.1:p.Ala25=
XR_001737282.1:n.200_209delinsCGCAGCCCGG
XR_002956997.1:n.200_209delinsCGCAGCCCGG
NM_001170535.3:c.74_83delinsCGCAGCCCGG MANE Select NP_001164006.1:p.Ala25=
NM_018188.5:c.74_83delinsCGCAGCCCGG NP_060658.3:p.Ala25=