Canonical Allele Identifier: CA2039029149
Gene: TSFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57796539C= , CM000674.2:g.57796539C= GRCh38
NC_000012.11:g.58190322C= , CM000674.1:g.58190322C= GRCh37
NC_000012.10:g.56476589C= NCBI36
NG_016971.1:g.18795C=

Transcript Alleles

HGVS Amino-acid change
ENST00000651066.1:c.*1076C= ENSP00000499143.1:n.*1076C=
ENST00000651284.1:c.*563C= ENSP00000499064.1:n.*563C=
ENST00000651899.1:c.*475C= ENSP00000498993.1:n.*475C=
ENST00000652027.2:c.934C= MANE Select ENSP00000499171.2:p.Arg312=
ENST00000323833.12:c.997C= ENSP00000313877.8:p.Arg333=
ENST00000454289.7:c.934C= ENSP00000388330.2:p.Arg312=
ENST00000540550.6:c.*342C= ENSP00000440987.1:n.*342C=
ENST00000543727.5:c.571+3466C= ENSP00000439342.1:n.571+3466C=
ENST00000548851.5:c.571+3466C= ENSP00000450041.1:n.571+3466C=
ENST00000550559.5:c.571+3466C= ENSP00000448575.1:n.571+3466C=
NM_001172695.1:c.*342C= NP_001166166.1:n.*342C=
NM_001172696.1:c.997C= NP_001166167.1:p.Arg333=
NM_001172697.1:c.571+3466C= NP_001166168.1:n.571+3466C=
NM_005726.5:c.934C= NP_005717.3:p.Arg312=
NM_001172695.2:c.*342C= NP_001166166.1:n.*342C=
NM_001172696.2:c.997C= NP_001166167.1:p.Arg333=
NM_005726.6:c.934C= MANE Select NP_005717.3:p.Arg312=
NM_001172697.2:c.571+3466C= NP_001166168.1:n.571+3466C=