Canonical Allele Identifier: CA2039028981
Gene: TSFM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57796449A= , CM000674.2:g.57796449A= GRCh38
NC_000012.11:g.58190232A= , CM000674.1:g.58190232A= GRCh37
NC_000012.10:g.56476499A= NCBI36
NG_016971.1:g.18705A=

Transcript Alleles

HGVS Amino-acid change
ENST00000651066.1:c.*986A= ENSP00000499143.1:n.*986A=
ENST00000651284.1:c.*473A= ENSP00000499064.1:n.*473A=
ENST00000651899.1:c.*385A= ENSP00000498993.1:n.*385A=
ENST00000652027.2:c.844A= MANE Select ENSP00000499171.2:p.Lys282=
ENST00000323833.12:c.907A= ENSP00000313877.8:p.Lys303=
ENST00000454289.7:c.844A= ENSP00000388330.2:p.Lys282=
ENST00000540550.6:c.*252A= ENSP00000440987.1:n.*252A=
ENST00000543727.5:c.571+3376A= ENSP00000439342.1:n.571+3376A=
ENST00000548851.5:c.571+3376A= ENSP00000450041.1:n.571+3376A=
ENST00000550559.5:c.571+3376A= ENSP00000448575.1:n.571+3376A=
NM_001172695.1:c.*252A= NP_001166166.1:n.*252A=
NM_001172696.1:c.907A= NP_001166167.1:p.Lys303=
NM_001172697.1:c.571+3376A= NP_001166168.1:n.571+3376A=
NM_005726.5:c.844A= NP_005717.3:p.Lys282=
NM_001172695.2:c.*252A= NP_001166166.1:n.*252A=
NM_001172696.2:c.907A= NP_001166167.1:p.Lys303=
NM_005726.6:c.844A= MANE Select NP_005717.3:p.Lys282=
NM_001172697.2:c.571+3376A= NP_001166168.1:n.571+3376A=