Canonical Allele Identifier: CA2276461789

Gene: SEPTIN9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77402357C= , CM000679.2:g.77402357C=	GRCh38
NC_000017.10:g.75398439C= , CM000679.1:g.75398439C=	GRCh37
NC_000017.9:g.72910034C=	NCBI36
NG_011683.1:g.125948C=
NG_011683.2:g.125948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.321C= MANE Plus Clinical	ENSP00000329161.8:p.Ile107=
ENST00000427177.6:c.375C= MANE Select	ENSP00000391249.1:p.Ile125=
ENST00000588690.6:c.-118C=	ENSP00000468668.1:n.-118C=
ENST00000590294.6:n.424C=
ENST00000329047.12:c.321C=	ENSP00000329161.8:p.Ile107=
ENST00000423034.6:c.354C=	ENSP00000405877.1:p.Ile118=
ENST00000427177.5:c.375C=	ENSP00000391249.1:p.Ile125=
ENST00000427674.6:c.-118C=	ENSP00000403194.1:n.-118C=
ENST00000431235.6:c.-118C=	ENSP00000406987.2:n.-118C=
ENST00000449803.6:c.-118C=	ENSP00000400181.2:n.-118C=
ENST00000586812.1:n.434C=
ENST00000587514.1:n.504C=
ENST00000588575.1:c.57C=	ENSP00000468090.1:p.Ile19=
ENST00000588690.5:c.-118C=	ENSP00000468668.1:n.-118C=
ENST00000589070.1:c.330C=	ENSP00000465332.1:p.Ile110=
ENST00000589140.1:c.330C=	ENSP00000466997.1:p.Ile110=
ENST00000590059.5:c.25-199C=	ENSP00000466164.1:n.25-199C=
ENST00000590294.5:c.321C=	ENSP00000465464.1:p.Ile107=
ENST00000590576.5:c.*375C=	ENSP00000465600.1:n.*375C=
ENST00000590586.1:n.480C=
ENST00000590595.1:c.57C=	ENSP00000465026.1:p.Ile19=
ENST00000590825.1:c.-118C=	ENSP00000468244.1:n.-118C=
ENST00000591198.5:c.318C=	ENSP00000468406.1:p.Ile106=
ENST00000591934.1:c.396C=	ENSP00000468504.1:p.Ile132=
ENST00000592098.1:n.405C=
ENST00000592420.1:c.-199C=	ENSP00000467051.1:n.-199C=
NM_001113491.1:c.375C=	NP_001106963.1:p.Ile125=
NM_001113492.1:c.-118C=	NP_001106964.1:n.-118C=
NM_001113493.1:c.354C=	NP_001106965.1:p.Ile118=
NM_001113494.1:c.-118C=	NP_001106966.1:n.-118C=
NM_001293695.1:c.318C=	NP_001280624.1:p.Ile106=
NM_006640.4:c.321C=	NP_006631.2:p.Ile107=
XM_006721643.2:c.-118C=	XP_006721706.1:n.-118C=
XM_011524204.1:c.468C=	XP_011522506.1:p.Ile156=
XM_011524205.1:c.465C=	XP_011522507.1:p.Ile155=
XM_011524206.1:c.330C=	XP_011522508.1:p.Ile110=
XM_011524207.1:c.-118C=	XP_011522509.1:n.-118C=
NM_001113491.2:c.375C= MANE Select	NP_001106963.1:p.Ile125=
NM_001113493.2:c.354C=	NP_001106965.1:p.Ile118=
NM_001293695.2:c.318C=	NP_001280624.1:p.Ile106=
NM_001113492.2:c.-118C=	NP_001106964.1:n.-118C=
NM_006640.5:c.321C= MANE Plus Clinical	NP_006631.2:p.Ile107=