Canonical Allele Identifier: CA889287104

Gene: ATAD3A

Linked Data

• dbSNP Id: rs1458935947
• gnomAD v3: 1-1512237-C-CCGGCGGCGGTAG
• gnomAD v4: 1-1512237-C-CCGGCGGCGGTAG
• MyVariant Identifiers: chr1:g.1447617_1447618insCGGCGGCGGTAG (hg19) ; chr1:g.1512237_1512238insCGGCGGCGGTAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1512247_1512258dup , CM000663.2:g.1512247_1512258dup	GRCh38
NC_000001.10:g.1447627_1447638dup , CM000663.1:g.1447627_1447638dup	GRCh37
NC_000001.9:g.1437490_1437501dup	NCBI36
NG_053035.1:g.5105_5116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378756.8:c.-22_-11dup MANE Select	ENSP00000368031.3:n.-22_-11dup
ENST00000672388.1:n.83_94dup
ENST00000378755.9:c.-22_-11dup	ENSP00000368030.5:n.-22_-11dup
ENST00000378756.7:c.-22_-11dup	ENSP00000368031.3:n.-22_-11dup
NM_001170535.1:c.-22_-11dup	NP_001164006.1:n.-22_-11dup
NM_018188.3:c.-22_-11dup	NP_060658.3:n.-22_-11dup
NM_001170535.2:c.-22_-11dup	NP_001164006.1:n.-22_-11dup
NM_018188.4:c.-22_-11dup	NP_060658.3:n.-22_-11dup
XM_024448098.1:c.-22_-11dup	XP_024303866.1:n.-22_-11dup
XR_001737282.1:n.105_116dup
XR_002956997.1:n.105_116dup
NM_001170535.3:c.-22_-11dup MANE Select	NP_001164006.1:n.-22_-11dup
NM_018188.5:c.-22_-11dup	NP_060658.3:n.-22_-11dup