Canonical Allele Identifier: CA485782098

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709479G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240273G>T , CM000676.2:g.24240273G>T	GRCh38
NC_000014.8:g.24709479G>T , CM000676.1:g.24709479G>T	GRCh37
NC_000014.7:g.23779319G>T	NCBI36
NG_016650.1:g.7402C>A
NG_054634.1:g.12857G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1510C>A
ENST00000557921.3:c.*142C>A	ENSP00000453157.3:n.*142C>A
ENST00000699682.1:n.1597C>A
ENST00000699683.1:n.1647C>A
ENST00000699684.1:c.*800C>A	ENSP00000514523.1:n.*800C>A
ENST00000699685.1:n.1411C>A
ENST00000699686.1:c.*142C>A	ENSP00000514524.1:n.*142C>A
ENST00000699687.1:c.*142C>A	ENSP00000514525.1:n.*142C>A
ENST00000699688.1:n.1407C>A
ENST00000699689.1:n.1763C>A
ENST00000699690.1:n.1960C>A
ENST00000699691.1:n.2104C>A
ENST00000699692.1:n.58C>A
ENST00000699693.1:n.1536C>A
ENST00000699694.1:n.1866C>A
ENST00000699695.1:c.*491C>A	ENSP00000514526.1:n.*491C>A
ENST00000699696.1:n.1510C>A
ENST00000699697.1:c.1119C>A	ENSP00000514527.1:p.Ala373=
ENST00000699698.1:n.1040C>A
ENST00000699699.1:n.1531C>A
ENST00000699700.1:n.1654C>A
ENST00000699701.1:c.*587C>A	ENSP00000514528.1:n.*587C>A
ENST00000267415.12:c.1119C>A MANE Select	ENSP00000267415.7:p.Ala373=
ENST00000646753.1:c.1014C>A	ENSP00000494065.1:p.Ala338=
ENST00000267415.11:c.1119C>A	ENSP00000267415.7:p.Ala373=
ENST00000399423.8:c.*142C>A	ENSP00000382350.4:n.*142C>A
ENST00000557915.1:n.326C>A
ENST00000558566.1:c.*579C>A	ENSP00000453025.1:n.*579C>A
ENST00000559969.5:c.965C>A
ENST00000560019.5:c.114C>A	ENSP00000453113.1:p.Ala38=
ENST00000626689.2:c.*491C>A	ENSP00000486681.1:n.*491C>A
NM_001099274.1:c.1119C>A	NP_001092744.1:p.Ala373=
NM_012461.2:c.*142C>A	NP_036593.2:n.*142C>A
XM_005267528.2:c.1119C>A	XP_005267585.1:p.Ala373=
XM_005267529.2:c.1014C>A	XP_005267586.1:p.Ala338=
NM_001099274.2:c.1119C>A	NP_001092744.1:p.Ala373=
NM_001363668.1:c.1014C>A	NP_001350597.1:p.Ala338=
NM_012461.3:c.*142C>A	NP_036593.2:n.*142C>A
XM_011536642.2:c.*587C>A	XP_011534944.1:n.*587C>A
XM_017021216.2:c.477C>A	XP_016876705.1:p.Ala159=
XM_017021217.1:c.477C>A	XP_016876706.1:p.Ala159=
NM_001099274.3:c.1119C>A MANE Select	NP_001092744.1:p.Ala373=
NM_001363668.2:c.1014C>A	NP_001350597.1:p.Ala338=