Canonical Allele Identifier: CA401206119

Gene: SEPTIN9

Linked Data

• MyVariant Identifiers: chr17:g.75398479G>C (hg19) ; chr17:g.77402397G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77402397G>C , CM000679.2:g.77402397G>C	GRCh38
NC_000017.10:g.75398479G>C , CM000679.1:g.75398479G>C	GRCh37
NC_000017.9:g.72910074G>C	NCBI36
NG_011683.1:g.125988G>C
NG_011683.2:g.125988G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.361G>C MANE Plus Clinical	ENSP00000329161.8:p.Gly121Arg
ENST00000427177.6:c.415G>C MANE Select	ENSP00000391249.1:p.Gly139Arg
ENST00000588690.6:c.-78G>C	ENSP00000468668.1:n.-78G>C
ENST00000590294.6:n.464G>C
ENST00000329047.12:c.361G>C	ENSP00000329161.8:p.Gly121Arg
ENST00000423034.6:c.394G>C	ENSP00000405877.1:p.Gly132Arg
ENST00000427177.5:c.415G>C	ENSP00000391249.1:p.Gly139Arg
ENST00000427674.6:c.-78G>C	ENSP00000403194.1:n.-78G>C
ENST00000431235.6:c.-78G>C	ENSP00000406987.2:n.-78G>C
ENST00000449803.6:c.-78G>C	ENSP00000400181.2:n.-78G>C
ENST00000588575.1:c.97G>C	ENSP00000468090.1:p.Gly33Arg
ENST00000588690.5:c.-78G>C	ENSP00000468668.1:n.-78G>C
ENST00000589070.1:c.370G>C	ENSP00000465332.1:p.Gly124Arg
ENST00000589140.1:c.370G>C	ENSP00000466997.1:p.Gly124Arg
ENST00000590059.5:c.25-159G>C	ENSP00000466164.1:n.25-159G>C
ENST00000590294.5:c.361G>C	ENSP00000465464.1:p.Gly121Arg
ENST00000590576.5:c.*415G>C	ENSP00000465600.1:n.*415G>C
ENST00000590586.1:n.520G>C
ENST00000590595.1:c.97G>C	ENSP00000465026.1:p.Gly33Arg
ENST00000590825.1:c.-78G>C	ENSP00000468244.1:n.-78G>C
ENST00000591198.5:c.358G>C	ENSP00000468406.1:p.Gly120Arg
ENST00000591934.1:c.436G>C	ENSP00000468504.1:p.Gly146Arg
ENST00000592098.1:n.445G>C
ENST00000592420.1:c.-159G>C	ENSP00000467051.1:n.-159G>C
NM_001113491.1:c.415G>C	NP_001106963.1:p.Gly139Arg
NM_001113492.1:c.-78G>C	NP_001106964.1:n.-78G>C
NM_001113493.1:c.394G>C	NP_001106965.1:p.Gly132Arg
NM_001113494.1:c.-78G>C	NP_001106966.1:n.-78G>C
NM_001293695.1:c.358G>C	NP_001280624.1:p.Gly120Arg
NM_006640.4:c.361G>C	NP_006631.2:p.Gly121Arg
XM_006721643.2:c.-78G>C	XP_006721706.1:n.-78G>C
XM_011524204.1:c.508G>C	XP_011522506.1:p.Gly170Arg
XM_011524205.1:c.505G>C	XP_011522507.1:p.Gly169Arg
XM_011524206.1:c.370G>C	XP_011522508.1:p.Gly124Arg
XM_011524207.1:c.-78G>C	XP_011522509.1:n.-78G>C
NM_001113491.2:c.415G>C MANE Select	NP_001106963.1:p.Gly139Arg
NM_001113493.2:c.394G>C	NP_001106965.1:p.Gly132Arg
NM_001293695.2:c.358G>C	NP_001280624.1:p.Gly120Arg
NM_001113492.2:c.-78G>C	NP_001106964.1:n.-78G>C
NM_006640.5:c.361G>C MANE Plus Clinical	NP_006631.2:p.Gly121Arg