Canonical Allele Identifier: CA385531031

Gene: TSFM

Linked Data

• MyVariant Identifiers: chr12:g.58190146G>C (hg19) ; chr12:g.57796363G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57796363G>C , CM000674.2:g.57796363G>C	GRCh38
NC_000012.11:g.58190146G>C , CM000674.1:g.58190146G>C	GRCh37
NC_000012.10:g.56476413G>C	NCBI36
NG_016971.1:g.18619G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651066.1:c.*900G>C	ENSP00000499143.1:n.*900G>C
ENST00000651284.1:c.*387G>C	ENSP00000499064.1:n.*387G>C
ENST00000651899.1:c.*299G>C	ENSP00000498993.1:n.*299G>C
ENST00000652027.2:c.758G>C MANE Select	ENSP00000499171.2:p.Gly253Ala
ENST00000323833.12:c.821G>C	ENSP00000313877.8:p.Gly274Ala
ENST00000454289.7:c.758G>C	ENSP00000388330.2:p.Gly253Ala
ENST00000497617.1:n.766G>C
ENST00000540550.6:c.*166G>C	ENSP00000440987.1:n.*166G>C
ENST00000543727.5:c.571+3290G>C	ENSP00000439342.1:n.571+3290G>C
ENST00000548851.5:c.571+3290G>C	ENSP00000450041.1:n.571+3290G>C
ENST00000550559.5:c.571+3290G>C	ENSP00000448575.1:n.571+3290G>C
NM_001172695.1:c.*166G>C	NP_001166166.1:n.*166G>C
NM_001172696.1:c.821G>C	NP_001166167.1:p.Gly274Ala
NM_001172697.1:c.571+3290G>C	NP_001166168.1:n.571+3290G>C
NM_005726.5:c.758G>C	NP_005717.3:p.Gly253Ala
NM_001172695.2:c.*166G>C	NP_001166166.1:n.*166G>C
NM_001172696.2:c.821G>C	NP_001166167.1:p.Gly274Ala
NM_005726.6:c.758G>C MANE Select	NP_005717.3:p.Gly253Ala
NM_001172697.2:c.571+3290G>C	NP_001166168.1:n.571+3290G>C