Canonical Allele Identifier: CA464394685
Gene: DNAI1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.34489329A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34489331A>T , CM000671.2:g.34489331A>T GRCh38
NC_000009.11:g.34489329A>T , CM000671.1:g.34489329A>T GRCh37
NC_000009.10:g.34479329A>T NCBI36
NG_008127.1:g.35519A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.270A>T MANE Select ENSP00000242317.4:p.Thr90=
ENST00000242317.8:c.270A>T ENSP00000242317.4:p.Thr90=
ENST00000437363.5:c.237A>T ENSP00000395396.1:p.Thr79=
ENST00000488369.1:n.386A>T
ENST00000614641.4:c.270A>T ENSP00000480538.1:p.Thr90=
NM_001281428.1:c.270A>T NP_001268357.1:p.Thr90=
NM_012144.3:c.270A>T NP_036276.1:p.Thr90=
XM_011517846.1:c.270A>T XP_011516148.1:p.Thr90=
XM_011517847.1:c.270A>T XP_011516149.1:p.Thr90=
XM_011517848.1:c.270A>T XP_011516150.1:p.Thr90=
XM_011517849.1:c.270A>T XP_011516151.1:p.Thr90=
XM_011517850.1:c.270A>T XP_011516152.1:p.Thr90=
XR_929232.1:n.524A>T
XR_929233.1:n.524A>T
XR_929235.1:n.524A>T
XM_006716758.3:c.-207A>T XP_006716821.1:n.-207A>T
XM_011517846.2:c.270A>T XP_011516148.1:p.Thr90=
XM_011517847.3:c.270A>T XP_011516149.1:p.Thr90=
XM_011517848.2:c.270A>T XP_011516150.1:p.Thr90=
XM_011517849.2:c.270A>T XP_011516151.1:p.Thr90=
XM_011517850.3:c.270A>T XP_011516152.1:p.Thr90=
XM_017014625.2:c.270A>T XP_016870114.1:p.Thr90=
XR_002956774.1:n.471A>T
XR_929232.2:n.471A>T
XR_929233.2:n.471A>T
NM_012144.4:c.270A>T MANE Select NP_036276.1:p.Thr90=
NM_001281428.2:c.270A>T NP_001268357.1:p.Thr90=