Canonical Allele Identifier: CA2276461718
Gene: SEPTIN9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.77402208C= , CM000679.2:g.77402208C= GRCh38
NC_000017.10:g.75398290C= , CM000679.1:g.75398290C= GRCh37
NC_000017.9:g.72909885C= NCBI36
NG_011683.1:g.125799C=
NG_011683.2:g.125799C=

Transcript Alleles

HGVS Amino-acid change
ENST00000329047.13:c.172C= MANE Plus Clinical ENSP00000329161.8:p.Arg58=
ENST00000427177.6:c.226C= MANE Select ENSP00000391249.1:p.Arg76=
ENST00000588690.6:c.-267C= ENSP00000468668.1:n.-267C=
ENST00000590294.6:n.275C=
ENST00000329047.12:c.172C= ENSP00000329161.8:p.Arg58=
ENST00000423034.6:c.205C= ENSP00000405877.1:p.Arg69=
ENST00000427177.5:c.226C= ENSP00000391249.1:p.Arg76=
ENST00000427674.6:c.-267C= ENSP00000403194.1:n.-267C=
ENST00000431235.6:c.-267C= ENSP00000406987.2:n.-267C=
ENST00000449803.6:c.-267C= ENSP00000400181.2:n.-267C=
ENST00000586812.1:n.285C=
ENST00000587514.1:n.355C=
ENST00000588575.1:c.37-129C= ENSP00000468090.1:n.37-129C=
ENST00000588690.5:c.-267C= ENSP00000468668.1:n.-267C=
ENST00000589070.1:c.181C= ENSP00000465332.1:p.Arg61=
ENST00000589140.1:c.181C= ENSP00000466997.1:p.Arg61=
ENST00000590059.5:c.25-348C= ENSP00000466164.1:n.25-348C=
ENST00000590294.5:c.172C= ENSP00000465464.1:p.Arg58=
ENST00000590576.5:c.*226C= ENSP00000465600.1:n.*226C=
ENST00000590586.1:n.331C=
ENST00000590595.1:c.37-129C= ENSP00000465026.1:n.37-129C=
ENST00000590825.1:c.-267C= ENSP00000468244.1:n.-267C=
ENST00000591198.5:c.169C= ENSP00000468406.1:p.Arg57=
ENST00000591833.5:c.*221C= ENSP00000466684.1:n.*221C=
ENST00000591934.1:c.247C= ENSP00000468504.1:p.Arg83=
ENST00000592098.1:n.256C=
ENST00000592420.1:c.-348C= ENSP00000467051.1:n.-348C=
NM_001113491.1:c.226C= NP_001106963.1:p.Arg76=
NM_001113492.1:c.-267C= NP_001106964.1:n.-267C=
NM_001113493.1:c.205C= NP_001106965.1:p.Arg69=
NM_001113494.1:c.-267C= NP_001106966.1:n.-267C=
NM_001293695.1:c.169C= NP_001280624.1:p.Arg57=
NM_006640.4:c.172C= NP_006631.2:p.Arg58=
XM_006721643.2:c.-267C= XP_006721706.1:n.-267C=
XM_011524204.1:c.319C= XP_011522506.1:p.Arg107=
XM_011524205.1:c.316C= XP_011522507.1:p.Arg106=
XM_011524206.1:c.181C= XP_011522508.1:p.Arg61=
XM_011524207.1:c.-267C= XP_011522509.1:n.-267C=
NM_001113491.2:c.226C= MANE Select NP_001106963.1:p.Arg76=
NM_001113493.2:c.205C= NP_001106965.1:p.Arg69=
NM_001293695.2:c.169C= NP_001280624.1:p.Arg57=
NM_001113492.2:c.-267C= NP_001106964.1:n.-267C=
NM_006640.5:c.172C= MANE Plus Clinical NP_006631.2:p.Arg58=