Canonical Allele Identifier: CA1123116693
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs1825186573

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517255_34517256del , CM000671.2:g.34517255_34517256del GRCh38
NC_000009.11:g.34517253_34517254del , CM000671.1:g.34517253_34517254del GRCh37
NC_000009.10:g.34507253_34507254del NCBI36
NG_008127.1:g.63443_63444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-30_1819-29del MANE Select ENSP00000242317.4:n.1819-30_1819-29del
ENST00000242317.8:c.1819-30_1819-29del ENSP00000242317.4:n.1819-30_1819-29del
ENST00000442556.1:c.329+2516_329+2517del
ENST00000470169.5:c.607-30_607-29del
ENST00000485580.1:n.395-30_395-29del
ENST00000614641.4:c.1831-30_1831-29del ENSP00000480538.1:n.1831-30_1831-29del
NM_001281428.1:c.1831-30_1831-29del NP_001268357.1:n.1831-30_1831-29del
NM_012144.3:c.1819-30_1819-29del NP_036276.1:n.1819-30_1819-29del
XM_006716758.2:c.1288-30_1288-29del XP_006716821.1:n.1288-30_1288-29del
XM_011517847.1:c.*25_*26del XP_011516149.1:n.*25_*26del
XM_011517848.1:c.1573-30_1573-29del XP_011516150.1:n.1573-30_1573-29del
XR_929233.1:n.2035_2036del
XM_006716758.3:c.1288-30_1288-29del XP_006716821.1:n.1288-30_1288-29del
XM_011517847.3:c.*25_*26del XP_011516149.1:n.*25_*26del
XM_011517848.2:c.1573-30_1573-29del XP_011516150.1:n.1573-30_1573-29del
XM_017014625.2:c.1561-30_1561-29del XP_016870114.1:n.1561-30_1561-29del
XR_002956774.1:n.1922-30_1922-29del
XR_929233.2:n.1982_1983del
NM_012144.4:c.1819-30_1819-29del MANE Select NP_036276.1:n.1819-30_1819-29del
NM_001281428.2:c.1831-30_1831-29del NP_001268357.1:n.1831-30_1831-29del