Canonical Allele Identifier: CA1845599401
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34506857T= , CM000671.2:g.34506857T= GRCh38
NC_000009.11:g.34506855T= , CM000671.1:g.34506855T= GRCh37
NC_000009.10:g.34496855T= NCBI36
NG_008127.1:g.53045T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1294T= MANE Select ENSP00000242317.4:p.Ser432=
ENST00000242317.8:c.1294T= ENSP00000242317.4:p.Ser432=
ENST00000470169.5:c.231T=
ENST00000614641.4:c.1306T= ENSP00000480538.1:p.Ser436=
NM_001281428.1:c.1306T= NP_001268357.1:p.Ser436=
NM_012144.3:c.1294T= NP_036276.1:p.Ser432=
XM_006716758.2:c.763T= XP_006716821.1:p.Ser255=
XM_011517846.1:c.1306T= XP_011516148.1:p.Ser436=
XM_011517847.1:c.1306T= XP_011516149.1:p.Ser436=
XM_011517848.1:c.1306T= XP_011516150.1:p.Ser436=
XM_011517849.1:c.1306T= XP_011516151.1:p.Ser436=
XM_011517850.1:c.1306T= XP_011516152.1:p.Ser436=
XR_929232.1:n.1560T=
XR_929233.1:n.1560T=
XR_929235.1:n.1560T=
XM_006716758.3:c.763T= XP_006716821.1:p.Ser255=
XM_011517846.2:c.1306T= XP_011516148.1:p.Ser436=
XM_011517847.3:c.1306T= XP_011516149.1:p.Ser436=
XM_011517848.2:c.1306T= XP_011516150.1:p.Ser436=
XM_011517849.2:c.1306T= XP_011516151.1:p.Ser436=
XM_011517850.3:c.1306T= XP_011516152.1:p.Ser436=
XM_017014625.2:c.1294T= XP_016870114.1:p.Ser432=
XR_002956774.1:n.1507T=
XR_929232.2:n.1507T=
XR_929233.2:n.1507T=
NM_012144.4:c.1294T= MANE Select NP_036276.1:p.Ser432=
NM_001281428.2:c.1306T= NP_001268357.1:p.Ser436=