Canonical Allele Identifier: CA2039028994

Gene: TSFM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57796458T= , CM000674.2:g.57796458T=	GRCh38
NC_000012.11:g.58190241T= , CM000674.1:g.58190241T=	GRCh37
NC_000012.10:g.56476508T=	NCBI36
NG_016971.1:g.18714T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651066.1:c.*995T=	ENSP00000499143.1:n.*995T=
ENST00000651284.1:c.*482T=	ENSP00000499064.1:n.*482T=
ENST00000651899.1:c.*394T=	ENSP00000498993.1:n.*394T=
ENST00000652027.2:c.853T= MANE Select	ENSP00000499171.2:p.Ser285=
ENST00000323833.12:c.916T=	ENSP00000313877.8:p.Ser306=
ENST00000454289.7:c.853T=	ENSP00000388330.2:p.Ser285=
ENST00000540550.6:c.*261T=	ENSP00000440987.1:n.*261T=
ENST00000543727.5:c.571+3385T=	ENSP00000439342.1:n.571+3385T=
ENST00000548851.5:c.571+3385T=	ENSP00000450041.1:n.571+3385T=
ENST00000550559.5:c.571+3385T=	ENSP00000448575.1:n.571+3385T=
NM_001172695.1:c.*261T=	NP_001166166.1:n.*261T=
NM_001172696.1:c.916T=	NP_001166167.1:p.Ser306=
NM_001172697.1:c.571+3385T=	NP_001166168.1:n.571+3385T=
NM_005726.5:c.853T=	NP_005717.3:p.Ser285=
NM_001172695.2:c.*261T=	NP_001166166.1:n.*261T=
NM_001172696.2:c.916T=	NP_001166167.1:p.Ser306=
NM_005726.6:c.853T= MANE Select	NP_005717.3:p.Ser285=
NM_001172697.2:c.571+3385T=	NP_001166168.1:n.571+3385T=