Canonical Allele Identifier: CA2039028986
Gene: TSFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57796453T= , CM000674.2:g.57796453T= GRCh38
NC_000012.11:g.58190236T= , CM000674.1:g.58190236T= GRCh37
NC_000012.10:g.56476503T= NCBI36
NG_016971.1:g.18709T=

Transcript Alleles

HGVS Amino-acid change
ENST00000651066.1:c.*990T= ENSP00000499143.1:n.*990T=
ENST00000651284.1:c.*477T= ENSP00000499064.1:n.*477T=
ENST00000651899.1:c.*389T= ENSP00000498993.1:n.*389T=
ENST00000652027.2:c.848T= MANE Select ENSP00000499171.2:p.Met283=
ENST00000323833.12:c.911T= ENSP00000313877.8:p.Met304=
ENST00000454289.7:c.848T= ENSP00000388330.2:p.Met283=
ENST00000540550.6:c.*256T= ENSP00000440987.1:n.*256T=
ENST00000543727.5:c.571+3380T= ENSP00000439342.1:n.571+3380T=
ENST00000548851.5:c.571+3380T= ENSP00000450041.1:n.571+3380T=
ENST00000550559.5:c.571+3380T= ENSP00000448575.1:n.571+3380T=
NM_001172695.1:c.*256T= NP_001166166.1:n.*256T=
NM_001172696.1:c.911T= NP_001166167.1:p.Met304=
NM_001172697.1:c.571+3380T= NP_001166168.1:n.571+3380T=
NM_005726.5:c.848T= NP_005717.3:p.Met283=
NM_001172695.2:c.*256T= NP_001166166.1:n.*256T=
NM_001172696.2:c.911T= NP_001166167.1:p.Met304=
NM_005726.6:c.848T= MANE Select NP_005717.3:p.Met283=
NM_001172697.2:c.571+3380T= NP_001166168.1:n.571+3380T=