Canonical Allele Identifier: CA2689798627

Gene: DNAI1

Linked Data

• gnomAD v4: 9-34517199-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517203del , CM000671.2:g.34517203del	GRCh38
NC_000009.11:g.34517201del , CM000671.1:g.34517201del	GRCh37
NC_000009.10:g.34507201del	NCBI36
NG_008127.1:g.63391del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-82del MANE Select	ENSP00000242317.4:n.1819-82del
ENST00000242317.8:c.1819-82del	ENSP00000242317.4:n.1819-82del
ENST00000442556.1:c.329+2464del
ENST00000470169.5:c.607-82del
ENST00000485580.1:n.395-82del
ENST00000614641.4:c.1831-82del	ENSP00000480538.1:n.1831-82del
NM_001281428.1:c.1831-82del	NP_001268357.1:n.1831-82del
NM_012144.3:c.1819-82del	NP_036276.1:n.1819-82del
XM_006716758.2:c.1288-82del	XP_006716821.1:n.1288-82del
XM_011517847.1:c.1839del	XP_011516149.1:p.Arg614GlyfsTer18
XM_011517848.1:c.1573-82del	XP_011516150.1:n.1573-82del
XR_929233.1:n.1983del
XM_006716758.3:c.1288-82del	XP_006716821.1:n.1288-82del
XM_011517847.3:c.1839del	XP_011516149.1:p.Arg614GlyfsTer18
XM_011517848.2:c.1573-82del	XP_011516150.1:n.1573-82del
XM_017014625.2:c.1561-82del	XP_016870114.1:n.1561-82del
XR_002956774.1:n.1922-82del
XR_929233.2:n.1930del
NM_012144.4:c.1819-82del MANE Select	NP_036276.1:n.1819-82del
NM_001281428.2:c.1831-82del	NP_001268357.1:n.1831-82del