Canonical Allele Identifier: CA521010203

Gene: ATAD3A

Linked Data

• dbSNP Id: rs1355758377
• gnomAD v2: 1-1447606-G-GGGTGGGGGTCCCGGCGGC
• gnomAD v3: 1-1512226-G-GGGTGGGGGTCCCGGCGGC
• gnomAD v4: 1-1512226-G-GGGTGGGGGTCCCGGCGGC
• MyVariant Identifiers: chr1:g.1447606_1447607insGGTGGGGGTCCCGGCGGC (hg19) ; chr1:g.1512226_1512227insGGTGGGGGTCCCGGCGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512230_1512247dup , CM000663.2:g.1512230_1512247dup	GRCh38
NC_000001.10:g.1447610_1447627dup , CM000663.1:g.1447610_1447627dup	GRCh37
NC_000001.9:g.1437473_1437490dup	NCBI36
NG_053035.1:g.5088_5105dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378756.8:c.-39_-22dup MANE Select	ENSP00000368031.3:n.-39_-22dup
ENST00000672388.1:n.66_83dup
ENST00000378755.9:c.-39_-22dup	ENSP00000368030.5:n.-39_-22dup
ENST00000378756.7:c.-39_-22dup	ENSP00000368031.3:n.-39_-22dup
NM_001170535.1:c.-39_-22dup	NP_001164006.1:n.-39_-22dup
NM_018188.3:c.-39_-22dup	NP_060658.3:n.-39_-22dup
NM_001170535.2:c.-39_-22dup	NP_001164006.1:n.-39_-22dup
NM_018188.4:c.-39_-22dup	NP_060658.3:n.-39_-22dup
XM_024448098.1:c.-39_-22dup	XP_024303866.1:n.-39_-22dup
XR_001737282.1:n.88_105dup
XR_002956997.1:n.88_105dup
NM_001170535.3:c.-39_-22dup MANE Select	NP_001164006.1:n.-39_-22dup
NM_018188.5:c.-39_-22dup	NP_060658.3:n.-39_-22dup