Canonical Allele Identifier: CA389224997

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709785A>T (hg19) ; chr14:g.24240579A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240579A>T , CM000676.2:g.24240579A>T	GRCh38
NC_000014.8:g.24709785A>T , CM000676.1:g.24709785A>T	GRCh37
NC_000014.7:g.23779625A>T	NCBI36
NG_016650.1:g.7096T>A
NG_054634.1:g.13163A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1204T>A
ENST00000557921.3:c.793T>A	ENSP00000453157.3:p.Ser265Thr
ENST00000699682.1:n.1291T>A
ENST00000699683.1:n.1341T>A
ENST00000699684.1:c.*494T>A	ENSP00000514523.1:n.*494T>A
ENST00000699685.1:n.1105T>A
ENST00000699686.1:c.694T>A	ENSP00000514524.1:p.Ser232Thr
ENST00000699687.1:c.796T>A	ENSP00000514525.1:p.Ser266Thr
ENST00000699688.1:n.1101T>A
ENST00000699689.1:n.1457T>A
ENST00000699690.1:n.1654T>A
ENST00000699691.1:n.1798T>A
ENST00000699693.1:n.1318T>A
ENST00000699694.1:n.1560T>A
ENST00000699695.1:c.*273T>A	ENSP00000514526.1:n.*273T>A
ENST00000699696.1:n.1204T>A
ENST00000699697.1:c.901T>A	ENSP00000514527.1:p.Ser301Thr
ENST00000699698.1:n.822T>A
ENST00000699699.1:n.1225T>A
ENST00000699700.1:n.1348T>A
ENST00000699701.1:c.*281T>A	ENSP00000514528.1:n.*281T>A
ENST00000267415.12:c.901T>A MANE Select	ENSP00000267415.7:p.Ser301Thr
ENST00000557921.2:c.793T>A	ENSP00000453157.2:p.Ser265Thr
ENST00000646753.1:c.796T>A	ENSP00000494065.1:p.Ser266Thr
ENST00000267415.11:c.901T>A	ENSP00000267415.7:p.Ser301Thr
ENST00000399423.8:c.901T>A	ENSP00000382350.4:p.Ser301Thr
ENST00000557915.1:n.20T>A
ENST00000558566.1:c.*273T>A	ENSP00000453025.1:n.*273T>A
ENST00000559019.1:c.*273T>A	ENSP00000453675.1:n.*273T>A
ENST00000559549.1:n.627T>A
ENST00000559969.5:c.758-99T>A
ENST00000626689.2:c.*273T>A	ENSP00000486681.1:n.*273T>A
NM_001099274.1:c.901T>A	NP_001092744.1:p.Ser301Thr
NM_012461.2:c.901T>A	NP_036593.2:p.Ser301Thr
XM_005267528.2:c.901T>A	XP_005267585.1:p.Ser301Thr
XM_005267529.2:c.796T>A	XP_005267586.1:p.Ser266Thr
NM_001099274.2:c.901T>A	NP_001092744.1:p.Ser301Thr
NM_001363668.1:c.796T>A	NP_001350597.1:p.Ser266Thr
NM_012461.3:c.901T>A	NP_036593.2:p.Ser301Thr
XM_011536642.2:c.*281T>A	XP_011534944.1:n.*281T>A
XM_017021216.2:c.259T>A	XP_016876705.1:p.Ser87Thr
XM_017021217.1:c.259T>A	XP_016876706.1:p.Ser87Thr
NM_001099274.3:c.901T>A MANE Select	NP_001092744.1:p.Ser301Thr
NM_001363668.2:c.796T>A	NP_001350597.1:p.Ser266Thr