Canonical Allele Identifier: CA2695210583
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34506794del , CM000671.2:g.34506794del GRCh38
NC_000009.11:g.34506792del , CM000671.1:g.34506792del GRCh37
NC_000009.10:g.34496792del NCBI36
NG_008127.1:g.52982del

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1231del MANE Select ENSP00000242317.4:p.Tyr411ThrfsTer?
ENST00000242317.8:c.1231del ENSP00000242317.4:p.Tyr411ThrfsTer?
ENST00000470169.5:c.168del
ENST00000614641.4:c.1243del ENSP00000480538.1:p.Tyr415ThrfsTer?
NM_001281428.1:c.1243del NP_001268357.1:p.Tyr415ThrfsTer?
NM_012144.3:c.1231del NP_036276.1:p.Tyr411ThrfsTer?
XM_006716758.2:c.700del XP_006716821.1:p.Tyr234ThrfsTer?
XM_011517846.1:c.1243del XP_011516148.1:p.Tyr415ThrfsTer?
XM_011517847.1:c.1243del XP_011516149.1:p.Tyr415ThrfsTer?
XM_011517848.1:c.1243del XP_011516150.1:p.Tyr415ThrfsTer?
XM_011517849.1:c.1243del XP_011516151.1:p.Tyr415ThrfsTer?
XM_011517850.1:c.1243del XP_011516152.1:p.Tyr415ThrfsTer?
XR_929232.1:n.1497del
XR_929233.1:n.1497del
XR_929235.1:n.1497del
XM_006716758.3:c.700del XP_006716821.1:p.Tyr234ThrfsTer?
XM_011517846.2:c.1243del XP_011516148.1:p.Tyr415ThrfsTer?
XM_011517847.3:c.1243del XP_011516149.1:p.Tyr415ThrfsTer?
XM_011517848.2:c.1243del XP_011516150.1:p.Tyr415ThrfsTer?
XM_011517849.2:c.1243del XP_011516151.1:p.Tyr415ThrfsTer?
XM_011517850.3:c.1243del XP_011516152.1:p.Tyr415ThrfsTer?
XM_017014625.2:c.1231del XP_016870114.1:p.Tyr411ThrfsTer?
XR_002956774.1:n.1444del
XR_929232.2:n.1444del
XR_929233.2:n.1444del
NM_012144.4:c.1231del MANE Select NP_036276.1:p.Tyr411ThrfsTer?
NM_001281428.2:c.1243del NP_001268357.1:p.Tyr415ThrfsTer?