Canonical Allele Identifier: CA1845592341
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517454G= , CM000671.2:g.34517454G= GRCh38
NC_000009.11:g.34517452G= , CM000671.1:g.34517452G= GRCh37
NC_000009.10:g.34507452G= NCBI36
NG_008127.1:g.63642G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1988G= MANE Select ENSP00000242317.4:p.Arg663=
ENST00000242317.8:c.1988G= ENSP00000242317.4:p.Arg663=
ENST00000442556.1:c.329+2715G=
ENST00000470169.5:c.776G=
ENST00000485580.1:n.564G=
ENST00000614641.4:c.2000G= ENSP00000480538.1:p.Arg667=
NM_001281428.1:c.2000G= NP_001268357.1:p.Arg667=
NM_012144.3:c.1988G= NP_036276.1:p.Arg663=
XM_006716758.2:c.1457G= XP_006716821.1:p.Arg486=
XM_011517848.1:c.1742G= XP_011516150.1:p.Arg581=
XM_006716758.3:c.1457G= XP_006716821.1:p.Arg486=
XM_011517848.2:c.1742G= XP_011516150.1:p.Arg581=
XM_017014625.2:c.1730G= XP_016870114.1:p.Arg577=
XR_002956774.1:n.2091G=
NM_012144.4:c.1988G= MANE Select NP_036276.1:p.Arg663=
NM_001281428.2:c.2000G= NP_001268357.1:p.Arg667=