Canonical Allele Identifier: CA2276422836

Gene: SEPTIN9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77320209_77320224delinsAGAGGAGGAGGAGGAG , CM000679.2:g.77320209_77320224delinsAGAGGAGGAGGAGGAG	GRCh38
NC_000017.10:g.75316291_75316306delinsAGAGGAGGAGGAGGAG , CM000679.1:g.75316291_75316306delinsAGAGGAGGAGGAGGAG	GRCh37
NC_000017.9:g.72827886_72827901delinsAGAGGAGGAGGAGGAG	NCBI36
NG_011683.1:g.43800_43815delinsAGAGGAGGAGGAGGAG
NG_011683.2:g.43800_43815delinsAGAGGAGGAGGAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.-118_-103delinsAGAGGAGGAGGAGGAG MANE Plus Clinical	ENSP00000329161.8:n.-118_-103delinsAGAGGAGGAGGAGGAG
ENST00000427177.6:c.76+13012_76+13027delinsAGAGGAGGAGGAGGAG MANE Select	ENSP00000391249.1:n.76+13012_76+13027delinsAGAGGAGGAGGAGGAG
ENST00000329047.12:c.-118_-103delinsAGAGGAGGAGGAGGAG	ENSP00000329161.8:n.-118_-103delinsAGAGGAGGAGGAGGAG
ENST00000427177.5:c.76+13012_76+13027delinsAGAGGAGGAGGAGGAG	ENSP00000391249.1:n.76+13012_76+13027delinsAGAGGAGGAGGAGGAG
ENST00000431235.6:c.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG	ENSP00000406987.2:n.-417+13012_-417+13027delinsAGAGGAGGAGGAGG...
ENST00000449803.6:c.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG	ENSP00000400181.2:n.-417+13012_-417+13027delinsAGAGGAGGAGGAGG...
ENST00000587237.1:n.406+13012_406+13027delinsAGAGGAGGAGGAGGAG
ENST00000588575.1:c.36+406_36+421delinsAGAGGAGGAGGAGGAG	ENSP00000468090.1:n.36+406_36+421delinsAGAGGAGGAGGAGGAG
ENST00000589070.1:c.31+39403_31+39418delinsAGAGGAGGAGGAGGAG	ENSP00000465332.1:n.31+39403_31+39418delinsAGAGGAGGAGGAGGAG
ENST00000590294.5:c.-118_-103delinsAGAGGAGGAGGAGGAG	ENSP00000465464.1:n.-118_-103delinsAGAGGAGGAGGAGGAG
ENST00000590576.5:c.*76+13012_*76+13027delinsAGAGGAGGAGGAGGAG	ENSP00000465600.1:n.*76+13012_*76+13027delinsAGAGGAGGAGGAGGAG...
ENST00000590595.1:c.36+406_36+421delinsAGAGGAGGAGGAGGAG	ENSP00000465026.1:n.36+406_36+421delinsAGAGGAGGAGGAGGAG
ENST00000591198.5:c.19+38655_19+38670delinsAGAGGAGGAGGAGGAG	ENSP00000468406.1:n.19+38655_19+38670delinsAGAGGAGGAGGAGGAG
ENST00000591833.5:c.*71+13012_*71+13027delinsAGAGGAGGAGGAGGAG	ENSP00000466684.1:n.*71+13012_*71+13027delinsAGAGGAGGAGGAGGAG...
NM_001113491.1:c.76+13012_76+13027delinsAGAGGAGGAGGAGGAG	NP_001106963.1:n.76+13012_76+13027delinsAGAGGAGGAGGAGGAG
NM_001113492.1:c.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG	NP_001106964.1:n.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG
NM_001293695.1:c.19+38655_19+38670delinsAGAGGAGGAGGAGGAG	NP_001280624.1:n.19+38655_19+38670delinsAGAGGAGGAGGAGGAG
NM_006640.4:c.-118_-103delinsAGAGGAGGAGGAGGAG	NP_006631.2:n.-118_-103delinsAGAGGAGGAGGAGGAG
XM_006721643.2:c.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG	XP_006721706.1:n.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG
XM_011524204.1:c.169+13012_169+13027delinsAGAGGAGGAGGAGGAG	XP_011522506.1:n.169+13012_169+13027delinsAGAGGAGGAGGAGGAG
XM_011524205.1:c.166+13012_166+13027delinsAGAGGAGGAGGAGGAG	XP_011522507.1:n.166+13012_166+13027delinsAGAGGAGGAGGAGGAG
NM_001113491.2:c.76+13012_76+13027delinsAGAGGAGGAGGAGGAG MANE Select	NP_001106963.1:n.76+13012_76+13027delinsAGAGGAGGAGGAGGAG
NM_001293695.2:c.19+38655_19+38670delinsAGAGGAGGAGGAGGAG	NP_001280624.1:n.19+38655_19+38670delinsAGAGGAGGAGGAGGAG
NM_001113492.2:c.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG	NP_001106964.1:n.-417+13012_-417+13027delinsAGAGGAGGAGGAGGAG
NM_006640.5:c.-118_-103delinsAGAGGAGGAGGAGGAG MANE Plus Clinical	NP_006631.2:n.-118_-103delinsAGAGGAGGAGGAGGAG