Canonical Allele Identifier: CA485782361

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709729G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240523G>T , CM000676.2:g.24240523G>T	GRCh38
NC_000014.8:g.24709729G>T , CM000676.1:g.24709729G>T	GRCh37
NC_000014.7:g.23779569G>T	NCBI36
NG_016650.1:g.7152C>A
NG_054634.1:g.13107G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1260C>A
ENST00000557921.3:c.849C>A	ENSP00000453157.3:p.Gly283=
ENST00000699682.1:n.1347C>A
ENST00000699683.1:n.1397C>A
ENST00000699684.1:c.*550C>A	ENSP00000514523.1:n.*550C>A
ENST00000699685.1:n.1161C>A
ENST00000699686.1:c.750C>A	ENSP00000514524.1:p.Gly250=
ENST00000699687.1:c.852C>A	ENSP00000514525.1:p.Gly284=
ENST00000699688.1:n.1157C>A
ENST00000699689.1:n.1513C>A
ENST00000699690.1:n.1710C>A
ENST00000699691.1:n.1854C>A
ENST00000699693.1:n.1374C>A
ENST00000699694.1:n.1616C>A
ENST00000699695.1:c.*329C>A	ENSP00000514526.1:n.*329C>A
ENST00000699696.1:n.1260C>A
ENST00000699697.1:c.957C>A	ENSP00000514527.1:p.Gly319=
ENST00000699698.1:n.878C>A
ENST00000699699.1:n.1281C>A
ENST00000699700.1:n.1404C>A
ENST00000699701.1:c.*337C>A	ENSP00000514528.1:n.*337C>A
ENST00000267415.12:c.957C>A MANE Select	ENSP00000267415.7:p.Gly319=
ENST00000557921.2:c.849C>A	ENSP00000453157.2:p.Gly283=
ENST00000646753.1:c.852C>A	ENSP00000494065.1:p.Gly284=
ENST00000267415.11:c.957C>A	ENSP00000267415.7:p.Gly319=
ENST00000399423.8:c.957C>A	ENSP00000382350.4:p.Gly319=
ENST00000557915.1:n.76C>A
ENST00000558566.1:c.*329C>A	ENSP00000453025.1:n.*329C>A
ENST00000559019.1:c.*329C>A	ENSP00000453675.1:n.*329C>A
ENST00000559969.5:c.758-43C>A
ENST00000626689.2:c.*329C>A	ENSP00000486681.1:n.*329C>A
NM_001099274.1:c.957C>A	NP_001092744.1:p.Gly319=
NM_012461.2:c.957C>A	NP_036593.2:p.Gly319=
XM_005267528.2:c.957C>A	XP_005267585.1:p.Gly319=
XM_005267529.2:c.852C>A	XP_005267586.1:p.Gly284=
NM_001099274.2:c.957C>A	NP_001092744.1:p.Gly319=
NM_001363668.1:c.852C>A	NP_001350597.1:p.Gly284=
NM_012461.3:c.957C>A	NP_036593.2:p.Gly319=
XM_011536642.2:c.*337C>A	XP_011534944.1:n.*337C>A
XM_017021216.2:c.315C>A	XP_016876705.1:p.Gly105=
XM_017021217.1:c.315C>A	XP_016876706.1:p.Gly105=
NM_001099274.3:c.957C>A MANE Select	NP_001092744.1:p.Gly319=
NM_001363668.2:c.852C>A	NP_001350597.1:p.Gly284=