Canonical Allele Identifier: CA2276461770
Gene: SEPTIN9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.77402314C= , CM000679.2:g.77402314C= GRCh38
NC_000017.10:g.75398396C= , CM000679.1:g.75398396C= GRCh37
NC_000017.9:g.72909991C= NCBI36
NG_011683.1:g.125905C=
NG_011683.2:g.125905C=

Transcript Alleles

HGVS Amino-acid change
ENST00000329047.13:c.278C= MANE Plus Clinical ENSP00000329161.8:p.Ser93=
ENST00000427177.6:c.332C= MANE Select ENSP00000391249.1:p.Ser111=
ENST00000588690.6:c.-161C= ENSP00000468668.1:n.-161C=
ENST00000590294.6:n.381C=
ENST00000329047.12:c.278C= ENSP00000329161.8:p.Ser93=
ENST00000423034.6:c.311C= ENSP00000405877.1:p.Ser104=
ENST00000427177.5:c.332C= ENSP00000391249.1:p.Ser111=
ENST00000427674.6:c.-161C= ENSP00000403194.1:n.-161C=
ENST00000431235.6:c.-161C= ENSP00000406987.2:n.-161C=
ENST00000449803.6:c.-161C= ENSP00000400181.2:n.-161C=
ENST00000586812.1:n.391C=
ENST00000587514.1:n.461C=
ENST00000588575.1:c.37-23C= ENSP00000468090.1:n.37-23C=
ENST00000588690.5:c.-161C= ENSP00000468668.1:n.-161C=
ENST00000589070.1:c.287C= ENSP00000465332.1:p.Ser96=
ENST00000589140.1:c.287C= ENSP00000466997.1:p.Ser96=
ENST00000590059.5:c.25-242C= ENSP00000466164.1:n.25-242C=
ENST00000590294.5:c.278C= ENSP00000465464.1:p.Ser93=
ENST00000590576.5:c.*332C= ENSP00000465600.1:n.*332C=
ENST00000590586.1:n.437C=
ENST00000590595.1:c.37-23C= ENSP00000465026.1:n.37-23C=
ENST00000590825.1:c.-161C= ENSP00000468244.1:n.-161C=
ENST00000591198.5:c.275C= ENSP00000468406.1:p.Ser92=
ENST00000591833.5:c.*327C= ENSP00000466684.1:n.*327C=
ENST00000591934.1:c.353C= ENSP00000468504.1:p.Ser118=
ENST00000592098.1:n.362C=
ENST00000592420.1:c.-242C= ENSP00000467051.1:n.-242C=
NM_001113491.1:c.332C= NP_001106963.1:p.Ser111=
NM_001113492.1:c.-161C= NP_001106964.1:n.-161C=
NM_001113493.1:c.311C= NP_001106965.1:p.Ser104=
NM_001113494.1:c.-161C= NP_001106966.1:n.-161C=
NM_001293695.1:c.275C= NP_001280624.1:p.Ser92=
NM_006640.4:c.278C= NP_006631.2:p.Ser93=
XM_006721643.2:c.-161C= XP_006721706.1:n.-161C=
XM_011524204.1:c.425C= XP_011522506.1:p.Ser142=
XM_011524205.1:c.422C= XP_011522507.1:p.Ser141=
XM_011524206.1:c.287C= XP_011522508.1:p.Ser96=
XM_011524207.1:c.-161C= XP_011522509.1:n.-161C=
NM_001113491.2:c.332C= MANE Select NP_001106963.1:p.Ser111=
NM_001113493.2:c.311C= NP_001106965.1:p.Ser104=
NM_001293695.2:c.275C= NP_001280624.1:p.Ser92=
NM_001113492.2:c.-161C= NP_001106964.1:n.-161C=
NM_006640.5:c.278C= MANE Plus Clinical NP_006631.2:p.Ser93=