Canonical Allele Identifier: CA587567964

Gene: DNAI1

Linked Data

• ClinVar Variation Id: 2898632
• ClinVar RCV Id: RCV003651354
• dbSNP Id: rs1368533559
• gnomAD v2: 9-34517264-G-A
• gnomAD v3: 9-34517266-G-A
• gnomAD v4: 9-34517266-G-A
• MyVariant Identifiers: chr9:g.34517264G>A (hg19) ; chr9:g.34517266G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517266G>A , CM000671.2:g.34517266G>A	GRCh38
NC_000009.11:g.34517264G>A , CM000671.1:g.34517264G>A	GRCh37
NC_000009.10:g.34507264G>A	NCBI36
NG_008127.1:g.63454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-19G>A MANE Select	ENSP00000242317.4:n.1819-19G>A
ENST00000242317.8:c.1819-19G>A	ENSP00000242317.4:n.1819-19G>A
ENST00000442556.1:c.329+2527G>A
ENST00000470169.5:c.607-19G>A
ENST00000485580.1:n.395-19G>A
ENST00000614641.4:c.1831-19G>A	ENSP00000480538.1:n.1831-19G>A
NM_001281428.1:c.1831-19G>A	NP_001268357.1:n.1831-19G>A
NM_012144.3:c.1819-19G>A	NP_036276.1:n.1819-19G>A
XM_006716758.2:c.1288-19G>A	XP_006716821.1:n.1288-19G>A
XM_011517847.1:c.*36G>A	XP_011516149.1:n.*36G>A
XM_011517848.1:c.1573-19G>A	XP_011516150.1:n.1573-19G>A
XR_929233.1:n.2046G>A
XM_006716758.3:c.1288-19G>A	XP_006716821.1:n.1288-19G>A
XM_011517847.3:c.*36G>A	XP_011516149.1:n.*36G>A
XM_011517848.2:c.1573-19G>A	XP_011516150.1:n.1573-19G>A
XM_017014625.2:c.1561-19G>A	XP_016870114.1:n.1561-19G>A
XR_002956774.1:n.1922-19G>A
XR_929233.2:n.1993G>A
NM_012144.4:c.1819-19G>A MANE Select	NP_036276.1:n.1819-19G>A
NM_001281428.2:c.1831-19G>A	NP_001268357.1:n.1831-19G>A