Canonical Allele Identifier: CA502069751

Gene: SEPTIN9

Linked Data

• MyVariant Identifiers: chr17:g.75398400T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77402318T>A , CM000679.2:g.77402318T>A	GRCh38
NC_000017.10:g.75398400T>A , CM000679.1:g.75398400T>A	GRCh37
NC_000017.9:g.72909995T>A	NCBI36
NG_011683.1:g.125909T>A
NG_011683.2:g.125909T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.282T>A MANE Plus Clinical	ENSP00000329161.8:p.Ile94=
ENST00000427177.6:c.336T>A MANE Select	ENSP00000391249.1:p.Ile112=
ENST00000588690.6:c.-157T>A	ENSP00000468668.1:n.-157T>A
ENST00000590294.6:n.385T>A
ENST00000329047.12:c.282T>A	ENSP00000329161.8:p.Ile94=
ENST00000423034.6:c.315T>A	ENSP00000405877.1:p.Ile105=
ENST00000427177.5:c.336T>A	ENSP00000391249.1:p.Ile112=
ENST00000427674.6:c.-157T>A	ENSP00000403194.1:n.-157T>A
ENST00000431235.6:c.-157T>A	ENSP00000406987.2:n.-157T>A
ENST00000449803.6:c.-157T>A	ENSP00000400181.2:n.-157T>A
ENST00000586812.1:n.395T>A
ENST00000587514.1:n.465T>A
ENST00000588575.1:c.37-19T>A	ENSP00000468090.1:n.37-19T>A
ENST00000588690.5:c.-157T>A	ENSP00000468668.1:n.-157T>A
ENST00000589070.1:c.291T>A	ENSP00000465332.1:p.Ile97=
ENST00000589140.1:c.291T>A	ENSP00000466997.1:p.Ile97=
ENST00000590059.5:c.25-238T>A	ENSP00000466164.1:n.25-238T>A
ENST00000590294.5:c.282T>A	ENSP00000465464.1:p.Ile94=
ENST00000590576.5:c.*336T>A	ENSP00000465600.1:n.*336T>A
ENST00000590586.1:n.441T>A
ENST00000590595.1:c.37-19T>A	ENSP00000465026.1:n.37-19T>A
ENST00000590825.1:c.-157T>A	ENSP00000468244.1:n.-157T>A
ENST00000591198.5:c.279T>A	ENSP00000468406.1:p.Ile93=
ENST00000591833.5:c.*331T>A	ENSP00000466684.1:n.*331T>A
ENST00000591934.1:c.357T>A	ENSP00000468504.1:p.Ile119=
ENST00000592098.1:n.366T>A
ENST00000592420.1:c.-238T>A	ENSP00000467051.1:n.-238T>A
NM_001113491.1:c.336T>A	NP_001106963.1:p.Ile112=
NM_001113492.1:c.-157T>A	NP_001106964.1:n.-157T>A
NM_001113493.1:c.315T>A	NP_001106965.1:p.Ile105=
NM_001113494.1:c.-157T>A	NP_001106966.1:n.-157T>A
NM_001293695.1:c.279T>A	NP_001280624.1:p.Ile93=
NM_006640.4:c.282T>A	NP_006631.2:p.Ile94=
XM_006721643.2:c.-157T>A	XP_006721706.1:n.-157T>A
XM_011524204.1:c.429T>A	XP_011522506.1:p.Ile143=
XM_011524205.1:c.426T>A	XP_011522507.1:p.Ile142=
XM_011524206.1:c.291T>A	XP_011522508.1:p.Ile97=
XM_011524207.1:c.-157T>A	XP_011522509.1:n.-157T>A
NM_001113491.2:c.336T>A MANE Select	NP_001106963.1:p.Ile112=
NM_001113493.2:c.315T>A	NP_001106965.1:p.Ile105=
NM_001293695.2:c.279T>A	NP_001280624.1:p.Ile93=
NM_001113492.2:c.-157T>A	NP_001106964.1:n.-157T>A
NM_006640.5:c.282T>A MANE Plus Clinical	NP_006631.2:p.Ile94=