Canonical Allele Identifier: CA1845591681
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517341G= , CM000671.2:g.34517341G= GRCh38
NC_000009.11:g.34517339G= , CM000671.1:g.34517339G= GRCh37
NC_000009.10:g.34507339G= NCBI36
NG_008127.1:g.63529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1875G= MANE Select ENSP00000242317.4:p.Val625=
ENST00000242317.8:c.1875G= ENSP00000242317.4:p.Val625=
ENST00000442556.1:c.329+2602G=
ENST00000470169.5:c.663G=
ENST00000485580.1:n.451G=
ENST00000614641.4:c.1887G= ENSP00000480538.1:p.Val629=
NM_001281428.1:c.1887G= NP_001268357.1:p.Val629=
NM_012144.3:c.1875G= NP_036276.1:p.Val625=
XM_006716758.2:c.1344G= XP_006716821.1:p.Val448=
XM_011517848.1:c.1629G= XP_011516150.1:p.Val543=
XM_006716758.3:c.1344G= XP_006716821.1:p.Val448=
XM_011517848.2:c.1629G= XP_011516150.1:p.Val543=
XM_017014625.2:c.1617G= XP_016870114.1:p.Val539=
XR_002956774.1:n.1978G=
NM_012144.4:c.1875G= MANE Select NP_036276.1:p.Val625=
NM_001281428.2:c.1887G= NP_001268357.1:p.Val629=