Canonical Allele Identifier: CA389223102

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709532A>T (hg19) ; chr14:g.24240326A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240326A>T , CM000676.2:g.24240326A>T	GRCh38
NC_000014.8:g.24709532A>T , CM000676.1:g.24709532A>T	GRCh37
NC_000014.7:g.23779372A>T	NCBI36
NG_016650.1:g.7349T>A
NG_054634.1:g.12910A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1457T>A
ENST00000557921.3:c.*89T>A	ENSP00000453157.3:n.*89T>A
ENST00000699682.1:n.1544T>A
ENST00000699683.1:n.1594T>A
ENST00000699684.1:c.*747T>A	ENSP00000514523.1:n.*747T>A
ENST00000699685.1:n.1358T>A
ENST00000699686.1:c.*89T>A	ENSP00000514524.1:n.*89T>A
ENST00000699687.1:c.*89T>A	ENSP00000514525.1:n.*89T>A
ENST00000699688.1:n.1354T>A
ENST00000699689.1:n.1710T>A
ENST00000699690.1:n.1907T>A
ENST00000699691.1:n.2051T>A
ENST00000699692.1:n.5T>A
ENST00000699693.1:n.1483T>A
ENST00000699694.1:n.1813T>A
ENST00000699695.1:c.*438T>A	ENSP00000514526.1:n.*438T>A
ENST00000699696.1:n.1457T>A
ENST00000699697.1:c.1066T>A	ENSP00000514527.1:p.Cys356Ser
ENST00000699698.1:n.987T>A
ENST00000699699.1:n.1478T>A
ENST00000699700.1:n.1601T>A
ENST00000699701.1:c.*534T>A	ENSP00000514528.1:n.*534T>A
ENST00000267415.12:c.1066T>A MANE Select	ENSP00000267415.7:p.Cys356Ser
ENST00000646753.1:c.961T>A	ENSP00000494065.1:p.Cys321Ser
ENST00000267415.11:c.1066T>A	ENSP00000267415.7:p.Cys356Ser
ENST00000399423.8:c.*89T>A	ENSP00000382350.4:n.*89T>A
ENST00000557915.1:n.273T>A
ENST00000558566.1:c.*526T>A	ENSP00000453025.1:n.*526T>A
ENST00000559969.5:c.912T>A
ENST00000560019.5:c.61T>A	ENSP00000453113.1:p.Cys21Ser
ENST00000626689.2:c.*438T>A	ENSP00000486681.1:n.*438T>A
NM_001099274.1:c.1066T>A	NP_001092744.1:p.Cys356Ser
NM_012461.2:c.*89T>A	NP_036593.2:n.*89T>A
XM_005267528.2:c.1066T>A	XP_005267585.1:p.Cys356Ser
XM_005267529.2:c.961T>A	XP_005267586.1:p.Cys321Ser
NM_001099274.2:c.1066T>A	NP_001092744.1:p.Cys356Ser
NM_001363668.1:c.961T>A	NP_001350597.1:p.Cys321Ser
NM_012461.3:c.*89T>A	NP_036593.2:n.*89T>A
XM_011536642.2:c.*534T>A	XP_011534944.1:n.*534T>A
XM_017021216.2:c.424T>A	XP_016876705.1:p.Cys142Ser
XM_017021217.1:c.424T>A	XP_016876706.1:p.Cys142Ser
NM_001099274.3:c.1066T>A MANE Select	NP_001092744.1:p.Cys356Ser
NM_001363668.2:c.961T>A	NP_001350597.1:p.Cys321Ser