Canonical Allele Identifier: CA485782167

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709864G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240658G>T , CM000676.2:g.24240658G>T	GRCh38
NC_000014.8:g.24709864G>T , CM000676.1:g.24709864G>T	GRCh37
NC_000014.7:g.23779704G>T	NCBI36
NG_016650.1:g.7017C>A
NG_054634.1:g.13242G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1125C>A
ENST00000557921.3:c.714C>A	ENSP00000453157.3:p.Ser238=
ENST00000699682.1:n.1212C>A
ENST00000699683.1:n.1262C>A
ENST00000699684.1:c.*415C>A	ENSP00000514523.1:n.*415C>A
ENST00000699685.1:n.1026C>A
ENST00000699686.1:c.615C>A	ENSP00000514524.1:p.Ser205=
ENST00000699687.1:c.717C>A	ENSP00000514525.1:p.Ser239=
ENST00000699688.1:n.1022C>A
ENST00000699689.1:n.1378C>A
ENST00000699690.1:n.1575C>A
ENST00000699691.1:n.1719C>A
ENST00000699693.1:n.1239C>A
ENST00000699694.1:n.1481C>A
ENST00000699695.1:c.*194C>A	ENSP00000514526.1:n.*194C>A
ENST00000699696.1:n.1125C>A
ENST00000699697.1:c.822C>A	ENSP00000514527.1:p.Ser274=
ENST00000699698.1:n.743C>A
ENST00000699699.1:n.1146C>A
ENST00000699700.1:n.1269C>A
ENST00000699701.1:c.*202C>A	ENSP00000514528.1:n.*202C>A
ENST00000267415.12:c.822C>A MANE Select	ENSP00000267415.7:p.Ser274=
ENST00000557921.2:c.714C>A	ENSP00000453157.2:p.Ser238=
ENST00000646753.1:c.717C>A	ENSP00000494065.1:p.Ser239=
ENST00000267415.11:c.822C>A	ENSP00000267415.7:p.Ser274=
ENST00000399423.8:c.822C>A	ENSP00000382350.4:p.Ser274=
ENST00000558476.5:c.384C>A	ENSP00000452724.1:p.Ser128=
ENST00000558566.1:c.*194C>A	ENSP00000453025.1:n.*194C>A
ENST00000559019.1:c.*194C>A	ENSP00000453675.1:n.*194C>A
ENST00000559549.1:n.548C>A
ENST00000559969.5:c.757+21C>A
ENST00000626689.2:c.*194C>A	ENSP00000486681.1:n.*194C>A
NM_001099274.1:c.822C>A	NP_001092744.1:p.Ser274=
NM_012461.2:c.822C>A	NP_036593.2:p.Ser274=
XM_005267528.2:c.822C>A	XP_005267585.1:p.Ser274=
XM_005267529.2:c.717C>A	XP_005267586.1:p.Ser239=
NM_001099274.2:c.822C>A	NP_001092744.1:p.Ser274=
NM_001363668.1:c.717C>A	NP_001350597.1:p.Ser239=
NM_012461.3:c.822C>A	NP_036593.2:p.Ser274=
XM_011536642.2:c.*202C>A	XP_011534944.1:n.*202C>A
XM_017021216.2:c.180C>A	XP_016876705.1:p.Ser60=
XM_017021217.1:c.180C>A	XP_016876706.1:p.Ser60=
NM_001099274.3:c.822C>A MANE Select	NP_001092744.1:p.Ser274=
NM_001363668.2:c.717C>A	NP_001350597.1:p.Ser239=