Canonical Allele Identifier: CA2276461731

Gene: SEPTIN9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77402235T= , CM000679.2:g.77402235T=	GRCh38
NC_000017.10:g.75398317T= , CM000679.1:g.75398317T=	GRCh37
NC_000017.9:g.72909912T=	NCBI36
NG_011683.1:g.125826T=
NG_011683.2:g.125826T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.199T= MANE Plus Clinical	ENSP00000329161.8:p.Ser67=
ENST00000427177.6:c.253T= MANE Select	ENSP00000391249.1:p.Ser85=
ENST00000588690.6:c.-240T=	ENSP00000468668.1:n.-240T=
ENST00000590294.6:n.302T=
ENST00000329047.12:c.199T=	ENSP00000329161.8:p.Ser67=
ENST00000423034.6:c.232T=	ENSP00000405877.1:p.Ser78=
ENST00000427177.5:c.253T=	ENSP00000391249.1:p.Ser85=
ENST00000427674.6:c.-240T=	ENSP00000403194.1:n.-240T=
ENST00000431235.6:c.-240T=	ENSP00000406987.2:n.-240T=
ENST00000449803.6:c.-240T=	ENSP00000400181.2:n.-240T=
ENST00000586812.1:n.312T=
ENST00000587514.1:n.382T=
ENST00000588575.1:c.37-102T=	ENSP00000468090.1:n.37-102T=
ENST00000588690.5:c.-240T=	ENSP00000468668.1:n.-240T=
ENST00000589070.1:c.208T=	ENSP00000465332.1:p.Ser70=
ENST00000589140.1:c.208T=	ENSP00000466997.1:p.Ser70=
ENST00000590059.5:c.25-321T=	ENSP00000466164.1:n.25-321T=
ENST00000590294.5:c.199T=	ENSP00000465464.1:p.Ser67=
ENST00000590576.5:c.*253T=	ENSP00000465600.1:n.*253T=
ENST00000590586.1:n.358T=
ENST00000590595.1:c.37-102T=	ENSP00000465026.1:n.37-102T=
ENST00000590825.1:c.-240T=	ENSP00000468244.1:n.-240T=
ENST00000591198.5:c.196T=	ENSP00000468406.1:p.Ser66=
ENST00000591833.5:c.*248T=	ENSP00000466684.1:n.*248T=
ENST00000591934.1:c.274T=	ENSP00000468504.1:p.Ser92=
ENST00000592098.1:n.283T=
ENST00000592420.1:c.-321T=	ENSP00000467051.1:n.-321T=
NM_001113491.1:c.253T=	NP_001106963.1:p.Ser85=
NM_001113492.1:c.-240T=	NP_001106964.1:n.-240T=
NM_001113493.1:c.232T=	NP_001106965.1:p.Ser78=
NM_001113494.1:c.-240T=	NP_001106966.1:n.-240T=
NM_001293695.1:c.196T=	NP_001280624.1:p.Ser66=
NM_006640.4:c.199T=	NP_006631.2:p.Ser67=
XM_006721643.2:c.-240T=	XP_006721706.1:n.-240T=
XM_011524204.1:c.346T=	XP_011522506.1:p.Ser116=
XM_011524205.1:c.343T=	XP_011522507.1:p.Ser115=
XM_011524206.1:c.208T=	XP_011522508.1:p.Ser70=
XM_011524207.1:c.-240T=	XP_011522509.1:n.-240T=
NM_001113491.2:c.253T= MANE Select	NP_001106963.1:p.Ser85=
NM_001113493.2:c.232T=	NP_001106965.1:p.Ser78=
NM_001293695.2:c.196T=	NP_001280624.1:p.Ser66=
NM_001113492.2:c.-240T=	NP_001106964.1:n.-240T=
NM_006640.5:c.199T= MANE Plus Clinical	NP_006631.2:p.Ser67=