Canonical Allele Identifier: CA1845608682
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34513121C= , CM000671.2:g.34513121C= GRCh38
NC_000009.11:g.34513119C= , CM000671.1:g.34513119C= GRCh37
NC_000009.10:g.34503119C= NCBI36
NG_008127.1:g.59309C=

Transcript Alleles

HGVS Amino-acid change
ENST00000242317.9:c.1499C= MANE Select ENSP00000242317.4:p.Thr500=
ENST00000242317.8:c.1499C= ENSP00000242317.4:p.Thr500=
ENST00000442556.1:c.10C=
ENST00000470169.5:c.436C=
ENST00000614641.4:c.1511C= ENSP00000480538.1:p.Thr504=
NM_001281428.1:c.1511C= NP_001268357.1:p.Thr504=
NM_012144.3:c.1499C= NP_036276.1:p.Thr500=
XM_006716758.2:c.968C= XP_006716821.1:p.Thr323=
XM_011517846.1:c.1511C= XP_011516148.1:p.Thr504=
XM_011517847.1:c.1511C= XP_011516149.1:p.Thr504=
XM_011517848.1:c.1324-1273C= XP_011516150.1:n.1324-1273C=
XM_011517849.1:c.1511C= XP_011516151.1:p.Thr504=
XR_929232.1:n.1765C=
XR_929233.1:n.1765C=
XR_929235.1:n.1578-1383C=
XM_006716758.3:c.968C= XP_006716821.1:p.Thr323=
XM_011517846.2:c.1511C= XP_011516148.1:p.Thr504=
XM_011517847.3:c.1511C= XP_011516149.1:p.Thr504=
XM_011517848.2:c.1324-1273C= XP_011516150.1:n.1324-1273C=
XM_011517849.2:c.1511C= XP_011516151.1:p.Thr504=
XM_017014625.2:c.1312-1273C= XP_016870114.1:n.1312-1273C=
XR_002956774.1:n.1712C=
XR_929232.2:n.1712C=
XR_929233.2:n.1712C=
NM_012144.4:c.1499C= MANE Select NP_036276.1:p.Thr500=
NM_001281428.2:c.1511C= NP_001268357.1:p.Thr504=