Canonical Allele Identifier: CA1845591843
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517365C= , CM000671.2:g.34517365C= GRCh38
NC_000009.11:g.34517363C= , CM000671.1:g.34517363C= GRCh37
NC_000009.10:g.34507363C= NCBI36
NG_008127.1:g.63553C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1899C= MANE Select ENSP00000242317.4:p.Thr633=
ENST00000242317.8:c.1899C= ENSP00000242317.4:p.Thr633=
ENST00000442556.1:c.329+2626C=
ENST00000470169.5:c.687C=
ENST00000485580.1:n.475C=
ENST00000614641.4:c.1911C= ENSP00000480538.1:p.Thr637=
NM_001281428.1:c.1911C= NP_001268357.1:p.Thr637=
NM_012144.3:c.1899C= NP_036276.1:p.Thr633=
XM_006716758.2:c.1368C= XP_006716821.1:p.Thr456=
XM_011517848.1:c.1653C= XP_011516150.1:p.Thr551=
XM_006716758.3:c.1368C= XP_006716821.1:p.Thr456=
XM_011517848.2:c.1653C= XP_011516150.1:p.Thr551=
XM_017014625.2:c.1641C= XP_016870114.1:p.Thr547=
XR_002956774.1:n.2002C=
NM_012144.4:c.1899C= MANE Select NP_036276.1:p.Thr633=
NM_001281428.2:c.1911C= NP_001268357.1:p.Thr637=