Canonical Allele Identifier: CA1845591237
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517194G= , CM000671.2:g.34517194G= GRCh38
NC_000009.11:g.34517192G= , CM000671.1:g.34517192G= GRCh37
NC_000009.10:g.34507192G= NCBI36
NG_008127.1:g.63382G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-91G= MANE Select ENSP00000242317.4:n.1819-91G=
ENST00000242317.8:c.1819-91G= ENSP00000242317.4:n.1819-91G=
ENST00000442556.1:c.329+2455G=
ENST00000470169.5:c.607-91G=
ENST00000485580.1:n.395-91G=
ENST00000614641.4:c.1831-91G= ENSP00000480538.1:n.1831-91G=
NM_001281428.1:c.1831-91G= NP_001268357.1:n.1831-91G=
NM_012144.3:c.1819-91G= NP_036276.1:n.1819-91G=
XM_006716758.2:c.1288-91G= XP_006716821.1:n.1288-91G=
XM_011517847.1:c.1831-1G= XP_011516149.1:n.1831-1G=
XM_011517848.1:c.1573-91G= XP_011516150.1:n.1573-91G=
XR_929233.1:n.1975-1G=
XM_006716758.3:c.1288-91G= XP_006716821.1:n.1288-91G=
XM_011517847.3:c.1831-1G= XP_011516149.1:n.1831-1G=
XM_011517848.2:c.1573-91G= XP_011516150.1:n.1573-91G=
XM_017014625.2:c.1561-91G= XP_016870114.1:n.1561-91G=
XR_002956774.1:n.1922-91G=
XR_929233.2:n.1922-1G=
NM_012144.4:c.1819-91G= MANE Select NP_036276.1:n.1819-91G=
NM_001281428.2:c.1831-91G= NP_001268357.1:n.1831-91G=