Canonical Allele Identifier: CA889287105

Gene: ATAD3A

Linked Data

• dbSNP Id: rs1198808900
• gnomAD v3: 1-1512238-C-T
• gnomAD v4: 1-1512238-C-T
• MyVariant Identifiers: chr1:g.1447618C>T (hg19) ; chr1:g.1512238C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512238C>T , CM000663.2:g.1512238C>T	GRCh38
NC_000001.10:g.1447618C>T , CM000663.1:g.1447618C>T	GRCh37
NC_000001.9:g.1437481C>T	NCBI36
NG_053035.1:g.5096C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378756.8:c.-31C>T MANE Select	ENSP00000368031.3:n.-31C>T
ENST00000672388.1:n.74C>T
ENST00000378755.9:c.-31C>T	ENSP00000368030.5:n.-31C>T
ENST00000378756.7:c.-31C>T	ENSP00000368031.3:n.-31C>T
NM_001170535.1:c.-31C>T	NP_001164006.1:n.-31C>T
NM_018188.3:c.-31C>T	NP_060658.3:n.-31C>T
NM_001170535.2:c.-31C>T	NP_001164006.1:n.-31C>T
NM_018188.4:c.-31C>T	NP_060658.3:n.-31C>T
XM_024448098.1:c.-31C>T	XP_024303866.1:n.-31C>T
XR_001737282.1:n.96C>T
XR_002956997.1:n.96C>T
NM_001170535.3:c.-31C>T MANE Select	NP_001164006.1:n.-31C>T
NM_018188.5:c.-31C>T	NP_060658.3:n.-31C>T