Canonical Allele Identifier: CA415385314
Gene: ATAD3A HGNC NCBI

Linked Data

gnomAD v4: 1-1512328-G-A
MyVariant Identifiers: chr1:g.1447708G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1512328G>A , CM000663.2:g.1512328G>A GRCh38
NC_000001.10:g.1447708G>A , CM000663.1:g.1447708G>A GRCh37
NC_000001.9:g.1437571G>A NCBI36
NG_053035.1:g.5186G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378756.8:c.60G>A MANE Select ENSP00000368031.3:p.Pro20=
ENST00000672388.1:n.164G>A
ENST00000378755.9:c.60G>A ENSP00000368030.5:p.Pro20=
ENST00000378756.7:c.60G>A ENSP00000368031.3:p.Pro20=
NM_001170535.1:c.60G>A NP_001164006.1:p.Pro20=
NM_018188.3:c.60G>A NP_060658.3:p.Pro20=
NM_001170535.2:c.60G>A NP_001164006.1:p.Pro20=
NM_018188.4:c.60G>A NP_060658.3:p.Pro20=
XM_024448098.1:c.60G>A XP_024303866.1:p.Pro20=
XR_001737282.1:n.186G>A
XR_002956997.1:n.186G>A
NM_001170535.3:c.60G>A MANE Select NP_001164006.1:p.Pro20=
NM_018188.5:c.60G>A NP_060658.3:p.Pro20=