Canonical Allele Identifier: CA2039029153
Gene: TSFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57796540G= , CM000674.2:g.57796540G= GRCh38
NC_000012.11:g.58190323G= , CM000674.1:g.58190323G= GRCh37
NC_000012.10:g.56476590G= NCBI36
NG_016971.1:g.18796G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651066.1:c.*1077G= ENSP00000499143.1:n.*1077G=
ENST00000651284.1:c.*564G= ENSP00000499064.1:n.*564G=
ENST00000651899.1:c.*476G= ENSP00000498993.1:n.*476G=
ENST00000652027.2:c.935G= MANE Select ENSP00000499171.2:p.Arg312=
ENST00000323833.12:c.998G= ENSP00000313877.8:p.Arg333=
ENST00000454289.7:c.935G= ENSP00000388330.2:p.Arg312=
ENST00000540550.6:c.*343G= ENSP00000440987.1:n.*343G=
ENST00000543727.5:c.571+3467G= ENSP00000439342.1:n.571+3467G=
ENST00000548851.5:c.571+3467G= ENSP00000450041.1:n.571+3467G=
ENST00000550559.5:c.571+3467G= ENSP00000448575.1:n.571+3467G=
NM_001172695.1:c.*343G= NP_001166166.1:n.*343G=
NM_001172696.1:c.998G= NP_001166167.1:p.Arg333=
NM_001172697.1:c.571+3467G= NP_001166168.1:n.571+3467G=
NM_005726.5:c.935G= NP_005717.3:p.Arg312=
NM_001172695.2:c.*343G= NP_001166166.1:n.*343G=
NM_001172696.2:c.998G= NP_001166167.1:p.Arg333=
NM_005726.6:c.935G= MANE Select NP_005717.3:p.Arg312=
NM_001172697.2:c.571+3467G= NP_001166168.1:n.571+3467G=