Canonical Allele Identifier: CA1149097830
Gene: ATAD3A HGNC NCBI

Linked Data

dbSNP Id: rs1274389321
gnomAD v4: 1-1512247-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512247T>C , CM000663.2:g.1512247T>C GRCh38
NC_000001.10:g.1447627T>C , CM000663.1:g.1447627T>C GRCh37
NC_000001.9:g.1437490T>C NCBI36
NG_053035.1:g.5105T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378756.8:c.-22T>C MANE Select ENSP00000368031.3:n.-22T>C
ENST00000672388.1:n.83T>C
ENST00000378755.9:c.-22T>C ENSP00000368030.5:n.-22T>C
ENST00000378756.7:c.-22T>C ENSP00000368031.3:n.-22T>C
NM_001170535.1:c.-22T>C NP_001164006.1:n.-22T>C
NM_018188.3:c.-22T>C NP_060658.3:n.-22T>C
NM_001170535.2:c.-22T>C NP_001164006.1:n.-22T>C
NM_018188.4:c.-22T>C NP_060658.3:n.-22T>C
XM_024448098.1:c.-22T>C XP_024303866.1:n.-22T>C
XR_001737282.1:n.105T>C
XR_002956997.1:n.105T>C
NM_001170535.3:c.-22T>C MANE Select NP_001164006.1:n.-22T>C
NM_018188.5:c.-22T>C NP_060658.3:n.-22T>C