Canonical Allele Identifier: CA2276461672
Gene: SEPTIN9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.77402115C= , CM000679.2:g.77402115C= GRCh38
NC_000017.10:g.75398197C= , CM000679.1:g.75398197C= GRCh37
NC_000017.9:g.72909792C= NCBI36
NG_011683.1:g.125706C=
NG_011683.2:g.125706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329047.13:c.79C= MANE Plus Clinical ENSP00000329161.8:p.Arg27=
ENST00000427177.6:c.133C= MANE Select ENSP00000391249.1:p.Arg45=
ENST00000588690.6:c.-360C= ENSP00000468668.1:n.-360C=
ENST00000590294.6:n.182C=
ENST00000329047.12:c.79C= ENSP00000329161.8:p.Arg27=
ENST00000423034.6:c.112C= ENSP00000405877.1:p.Arg38=
ENST00000427177.5:c.133C= ENSP00000391249.1:p.Arg45=
ENST00000427674.6:c.-360C= ENSP00000403194.1:n.-360C=
ENST00000431235.6:c.-360C= ENSP00000406987.2:n.-360C=
ENST00000449803.6:c.-360C= ENSP00000400181.2:n.-360C=
ENST00000586812.1:n.192C=
ENST00000587237.1:n.463C=
ENST00000587514.1:n.262C=
ENST00000588575.1:c.37-222C= ENSP00000468090.1:n.37-222C=
ENST00000588690.5:c.-360C= ENSP00000468668.1:n.-360C=
ENST00000589070.1:c.88C= ENSP00000465332.1:p.Arg30=
ENST00000589140.1:c.88C= ENSP00000466997.1:p.Arg30=
ENST00000590059.5:c.25-441C= ENSP00000466164.1:n.25-441C=
ENST00000590294.5:c.79C= ENSP00000465464.1:p.Arg27=
ENST00000590576.5:c.*133C= ENSP00000465600.1:n.*133C=
ENST00000590586.1:n.238C=
ENST00000590595.1:c.37-222C= ENSP00000465026.1:n.37-222C=
ENST00000590825.1:c.-360C= ENSP00000468244.1:n.-360C=
ENST00000591198.5:c.76C= ENSP00000468406.1:p.Arg26=
ENST00000591833.5:c.*128C= ENSP00000466684.1:n.*128C=
ENST00000591934.1:c.154C= ENSP00000468504.1:p.Arg52=
ENST00000592098.1:n.163C=
ENST00000592420.1:c.-441C= ENSP00000467051.1:n.-441C=
NM_001113491.1:c.133C= NP_001106963.1:p.Arg45=
NM_001113492.1:c.-360C= NP_001106964.1:n.-360C=
NM_001113493.1:c.112C= NP_001106965.1:p.Arg38=
NM_001113494.1:c.-360C= NP_001106966.1:n.-360C=
NM_001293695.1:c.76C= NP_001280624.1:p.Arg26=
NM_006640.4:c.79C= NP_006631.2:p.Arg27=
XM_006721643.2:c.-360C= XP_006721706.1:n.-360C=
XM_011524204.1:c.226C= XP_011522506.1:p.Arg76=
XM_011524205.1:c.223C= XP_011522507.1:p.Arg75=
XM_011524206.1:c.88C= XP_011522508.1:p.Arg30=
XM_011524207.1:c.-360C= XP_011522509.1:n.-360C=
NM_001113491.2:c.133C= MANE Select NP_001106963.1:p.Arg45=
NM_001113493.2:c.112C= NP_001106965.1:p.Arg38=
NM_001293695.2:c.76C= NP_001280624.1:p.Arg26=
NM_001113492.2:c.-360C= NP_001106964.1:n.-360C=
NM_006640.5:c.79C= MANE Plus Clinical NP_006631.2:p.Arg27=