Canonical Allele Identifier: CA2276422662

Gene: SEPTIN9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.77319871C= , CM000679.2:g.77319871C=	GRCh38
NC_000017.10:g.75315953C= , CM000679.1:g.75315953C=	GRCh37
NC_000017.9:g.72827548C=	NCBI36
NG_011683.1:g.43462C=
NG_011683.2:g.43462C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329047.13:c.-456C= MANE Plus Clinical	ENSP00000329161.8:n.-456C=
ENST00000427177.6:c.76+12674C= MANE Select	ENSP00000391249.1:n.76+12674C=
ENST00000329047.12:c.-456C=	ENSP00000329161.8:n.-456C=
ENST00000427177.5:c.76+12674C=	ENSP00000391249.1:n.76+12674C=
ENST00000431235.6:c.-417+12674C=	ENSP00000406987.2:n.-417+12674C=
ENST00000449803.6:c.-417+12674C=	ENSP00000400181.2:n.-417+12674C=
ENST00000587237.1:n.406+12674C=
ENST00000588575.1:c.36+68C=	ENSP00000468090.1:n.36+68C=
ENST00000589070.1:c.31+39065C=	ENSP00000465332.1:n.31+39065C=
ENST00000590294.5:c.-456C=	ENSP00000465464.1:n.-456C=
ENST00000590576.5:c.*76+12674C=	ENSP00000465600.1:n.*76+12674C=
ENST00000590595.1:c.36+68C=	ENSP00000465026.1:n.36+68C=
ENST00000591198.5:c.19+38317C=	ENSP00000468406.1:n.19+38317C=
ENST00000591833.5:c.*71+12674C=	ENSP00000466684.1:n.*71+12674C=
NM_001113491.1:c.76+12674C=	NP_001106963.1:n.76+12674C=
NM_001113492.1:c.-417+12674C=	NP_001106964.1:n.-417+12674C=
NM_001293695.1:c.19+38317C=	NP_001280624.1:n.19+38317C=
NM_006640.4:c.-456C=	NP_006631.2:n.-456C=
XM_006721643.2:c.-417+12674C=	XP_006721706.1:n.-417+12674C=
XM_011524204.1:c.169+12674C=	XP_011522506.1:n.169+12674C=
XM_011524205.1:c.166+12674C=	XP_011522507.1:n.166+12674C=
NM_001113491.2:c.76+12674C= MANE Select	NP_001106963.1:n.76+12674C=
NM_001293695.2:c.19+38317C=	NP_001280624.1:n.19+38317C=
NM_001113492.2:c.-417+12674C=	NP_001106964.1:n.-417+12674C=
NM_006640.5:c.-456C= MANE Plus Clinical	NP_006631.2:n.-456C=