Canonical Allele Identifier: CA385531627

Gene: TSFM

Linked Data

• MyVariant Identifiers: chr12:g.58190229A>T (hg19) ; chr12:g.57796446A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57796446A>T , CM000674.2:g.57796446A>T	GRCh38
NC_000012.11:g.58190229A>T , CM000674.1:g.58190229A>T	GRCh37
NC_000012.10:g.56476496A>T	NCBI36
NG_016971.1:g.18702A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651066.1:c.*983A>T	ENSP00000499143.1:n.*983A>T
ENST00000651284.1:c.*470A>T	ENSP00000499064.1:n.*470A>T
ENST00000651899.1:c.*382A>T	ENSP00000498993.1:n.*382A>T
ENST00000652027.2:c.841A>T MANE Select	ENSP00000499171.2:p.Thr281Ser
ENST00000323833.12:c.904A>T	ENSP00000313877.8:p.Thr302Ser
ENST00000454289.7:c.841A>T	ENSP00000388330.2:p.Thr281Ser
ENST00000540550.6:c.*249A>T	ENSP00000440987.1:n.*249A>T
ENST00000543727.5:c.571+3373A>T	ENSP00000439342.1:n.571+3373A>T
ENST00000548851.5:c.571+3373A>T	ENSP00000450041.1:n.571+3373A>T
ENST00000550559.5:c.571+3373A>T	ENSP00000448575.1:n.571+3373A>T
NM_001172695.1:c.*249A>T	NP_001166166.1:n.*249A>T
NM_001172696.1:c.904A>T	NP_001166167.1:p.Thr302Ser
NM_001172697.1:c.571+3373A>T	NP_001166168.1:n.571+3373A>T
NM_005726.5:c.841A>T	NP_005717.3:p.Thr281Ser
NM_001172695.2:c.*249A>T	NP_001166166.1:n.*249A>T
NM_001172696.2:c.904A>T	NP_001166167.1:p.Thr302Ser
NM_005726.6:c.841A>T MANE Select	NP_005717.3:p.Thr281Ser
NM_001172697.2:c.571+3373A>T	NP_001166168.1:n.571+3373A>T