Canonical Allele Identifier: CA521010208

Gene: ATAD3A

Linked Data

• dbSNP Id: rs1469501800
• gnomAD v2: 1-1447613-G-A
• gnomAD v3: 1-1512233-G-A
• gnomAD v4: 1-1512233-G-A
• MyVariant Identifiers: chr1:g.1447613G>A (hg19) ; chr1:g.1512233G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512233G>A , CM000663.2:g.1512233G>A	GRCh38
NC_000001.10:g.1447613G>A , CM000663.1:g.1447613G>A	GRCh37
NC_000001.9:g.1437476G>A	NCBI36
NG_053035.1:g.5091G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378756.8:c.-36G>A MANE Select	ENSP00000368031.3:n.-36G>A
ENST00000672388.1:n.69G>A
ENST00000378755.9:c.-36G>A	ENSP00000368030.5:n.-36G>A
ENST00000378756.7:c.-36G>A	ENSP00000368031.3:n.-36G>A
NM_001170535.1:c.-36G>A	NP_001164006.1:n.-36G>A
NM_018188.3:c.-36G>A	NP_060658.3:n.-36G>A
NM_001170535.2:c.-36G>A	NP_001164006.1:n.-36G>A
NM_018188.4:c.-36G>A	NP_060658.3:n.-36G>A
XM_024448098.1:c.-36G>A	XP_024303866.1:n.-36G>A
XR_001737282.1:n.91G>A
XR_002956997.1:n.91G>A
NM_001170535.3:c.-36G>A MANE Select	NP_001164006.1:n.-36G>A
NM_018188.5:c.-36G>A	NP_060658.3:n.-36G>A