Canonical Allele Identifier: CA2579327436
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34513018_34513019del , CM000671.2:g.34513018_34513019del GRCh38
NC_000009.11:g.34513016_34513017del , CM000671.1:g.34513016_34513017del GRCh37
NC_000009.10:g.34503016_34503017del NCBI36
NG_008127.1:g.59206_59207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1490-94_1490-93del MANE Select ENSP00000242317.4:n.1490-94_1490-93del
ENST00000242317.8:c.1490-94_1490-93del ENSP00000242317.4:n.1490-94_1490-93del
ENST00000470169.5:c.427-94_427-93del
ENST00000614641.4:c.1502-94_1502-93del ENSP00000480538.1:n.1502-94_1502-93del
NM_001281428.1:c.1502-94_1502-93del NP_001268357.1:n.1502-94_1502-93del
NM_012144.3:c.1490-94_1490-93del NP_036276.1:n.1490-94_1490-93del
XM_006716758.2:c.959-94_959-93del XP_006716821.1:n.959-94_959-93del
XM_011517846.1:c.1502-94_1502-93del XP_011516148.1:n.1502-94_1502-93del
XM_011517847.1:c.1502-94_1502-93del XP_011516149.1:n.1502-94_1502-93del
XM_011517848.1:c.1324-1376_1324-1375del XP_011516150.1:n.1324-1376_1324-1375del
XM_011517849.1:c.1502-94_1502-93del XP_011516151.1:n.1502-94_1502-93del
XR_929232.1:n.1756-94_1756-93del
XR_929233.1:n.1756-94_1756-93del
XR_929235.1:n.1578-1486_1578-1485del
XM_006716758.3:c.959-94_959-93del XP_006716821.1:n.959-94_959-93del
XM_011517846.2:c.1502-94_1502-93del XP_011516148.1:n.1502-94_1502-93del
XM_011517847.3:c.1502-94_1502-93del XP_011516149.1:n.1502-94_1502-93del
XM_011517848.2:c.1324-1376_1324-1375del XP_011516150.1:n.1324-1376_1324-1375del
XM_011517849.2:c.1502-94_1502-93del XP_011516151.1:n.1502-94_1502-93del
XM_017014625.2:c.1312-1376_1312-1375del XP_016870114.1:n.1312-1376_1312-1375del
XR_002956774.1:n.1703-94_1703-93del
XR_929232.2:n.1703-94_1703-93del
XR_929233.2:n.1703-94_1703-93del
NM_012144.4:c.1490-94_1490-93del MANE Select NP_036276.1:n.1490-94_1490-93del
NM_001281428.2:c.1502-94_1502-93del NP_001268357.1:n.1502-94_1502-93del