Canonical Allele Identifier: CA385531588

Gene: TSFM

Linked Data

• MyVariant Identifiers: chr12:g.58190224C>T (hg19) ; chr12:g.57796441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57796441C>T , CM000674.2:g.57796441C>T	GRCh38
NC_000012.11:g.58190224C>T , CM000674.1:g.58190224C>T	GRCh37
NC_000012.10:g.56476491C>T	NCBI36
NG_016971.1:g.18697C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651066.1:c.*978C>T	ENSP00000499143.1:n.*978C>T
ENST00000651284.1:c.*465C>T	ENSP00000499064.1:n.*465C>T
ENST00000651899.1:c.*377C>T	ENSP00000498993.1:n.*377C>T
ENST00000652027.2:c.836C>T MANE Select	ENSP00000499171.2:p.Ala279Val
ENST00000323833.12:c.899C>T	ENSP00000313877.8:p.Ala300Val
ENST00000454289.7:c.836C>T	ENSP00000388330.2:p.Ala279Val
ENST00000540550.6:c.*244C>T	ENSP00000440987.1:n.*244C>T
ENST00000543727.5:c.571+3368C>T	ENSP00000439342.1:n.571+3368C>T
ENST00000548851.5:c.571+3368C>T	ENSP00000450041.1:n.571+3368C>T
ENST00000550559.5:c.571+3368C>T	ENSP00000448575.1:n.571+3368C>T
NM_001172695.1:c.*244C>T	NP_001166166.1:n.*244C>T
NM_001172696.1:c.899C>T	NP_001166167.1:p.Ala300Val
NM_001172697.1:c.571+3368C>T	NP_001166168.1:n.571+3368C>T
NM_005726.5:c.836C>T	NP_005717.3:p.Ala279Val
NM_001172695.2:c.*244C>T	NP_001166166.1:n.*244C>T
NM_001172696.2:c.899C>T	NP_001166167.1:p.Ala300Val
NM_005726.6:c.836C>T MANE Select	NP_005717.3:p.Ala279Val
NM_001172697.2:c.571+3368C>T	NP_001166168.1:n.571+3368C>T