Canonical Allele Identifier: CA502069558

Gene: SEPTIN9

Linked Data

• MyVariant Identifiers: chr17:g.75398190C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77402108C>T , CM000679.2:g.77402108C>T	GRCh38
NC_000017.10:g.75398190C>T , CM000679.1:g.75398190C>T	GRCh37
NC_000017.9:g.72909785C>T	NCBI36
NG_011683.1:g.125699C>T
NG_011683.2:g.125699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.72C>T MANE Plus Clinical	ENSP00000329161.8:p.Thr24=
ENST00000427177.6:c.126C>T MANE Select	ENSP00000391249.1:p.Thr42=
ENST00000588690.6:c.-367C>T	ENSP00000468668.1:n.-367C>T
ENST00000590294.6:n.175C>T
ENST00000329047.12:c.72C>T	ENSP00000329161.8:p.Thr24=
ENST00000423034.6:c.105C>T	ENSP00000405877.1:p.Thr35=
ENST00000427177.5:c.126C>T	ENSP00000391249.1:p.Thr42=
ENST00000427674.6:c.-367C>T	ENSP00000403194.1:n.-367C>T
ENST00000431235.6:c.-367C>T	ENSP00000406987.2:n.-367C>T
ENST00000449803.6:c.-367C>T	ENSP00000400181.2:n.-367C>T
ENST00000586812.1:n.185C>T
ENST00000587237.1:n.456C>T
ENST00000587514.1:n.255C>T
ENST00000588575.1:c.37-229C>T	ENSP00000468090.1:n.37-229C>T
ENST00000588690.5:c.-367C>T	ENSP00000468668.1:n.-367C>T
ENST00000589070.1:c.81C>T	ENSP00000465332.1:p.Thr27=
ENST00000589140.1:c.81C>T	ENSP00000466997.1:p.Thr27=
ENST00000590059.5:c.25-448C>T	ENSP00000466164.1:n.25-448C>T
ENST00000590294.5:c.72C>T	ENSP00000465464.1:p.Thr24=
ENST00000590576.5:c.*126C>T	ENSP00000465600.1:n.*126C>T
ENST00000590586.1:n.231C>T
ENST00000590595.1:c.37-229C>T	ENSP00000465026.1:n.37-229C>T
ENST00000590825.1:c.-367C>T	ENSP00000468244.1:n.-367C>T
ENST00000591198.5:c.69C>T	ENSP00000468406.1:p.Thr23=
ENST00000591833.5:c.*121C>T	ENSP00000466684.1:n.*121C>T
ENST00000591934.1:c.147C>T	ENSP00000468504.1:p.Thr49=
ENST00000592098.1:n.156C>T
ENST00000592420.1:c.-448C>T	ENSP00000467051.1:n.-448C>T
NM_001113491.1:c.126C>T	NP_001106963.1:p.Thr42=
NM_001113492.1:c.-367C>T	NP_001106964.1:n.-367C>T
NM_001113493.1:c.105C>T	NP_001106965.1:p.Thr35=
NM_001113494.1:c.-367C>T	NP_001106966.1:n.-367C>T
NM_001293695.1:c.69C>T	NP_001280624.1:p.Thr23=
NM_006640.4:c.72C>T	NP_006631.2:p.Thr24=
XM_006721643.2:c.-367C>T	XP_006721706.1:n.-367C>T
XM_011524204.1:c.219C>T	XP_011522506.1:p.Thr73=
XM_011524205.1:c.216C>T	XP_011522507.1:p.Thr72=
XM_011524206.1:c.81C>T	XP_011522508.1:p.Thr27=
XM_011524207.1:c.-367C>T	XP_011522509.1:n.-367C>T
NM_001113491.2:c.126C>T MANE Select	NP_001106963.1:p.Thr42=
NM_001113493.2:c.105C>T	NP_001106965.1:p.Thr35=
NM_001293695.2:c.69C>T	NP_001280624.1:p.Thr23=
NM_001113492.2:c.-367C>T	NP_001106964.1:n.-367C>T
NM_006640.5:c.72C>T MANE Plus Clinical	NP_006631.2:p.Thr24=