Canonical Allele Identifier: CA485782295

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709699C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240493C>T , CM000676.2:g.24240493C>T	GRCh38
NC_000014.8:g.24709699C>T , CM000676.1:g.24709699C>T	GRCh37
NC_000014.7:g.23779539C>T	NCBI36
NG_016650.1:g.7182G>A
NG_054634.1:g.13077C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1290G>A
ENST00000557921.3:c.879G>A	ENSP00000453157.3:p.Lys293=
ENST00000699682.1:n.1377G>A
ENST00000699683.1:n.1427G>A
ENST00000699684.1:c.*580G>A	ENSP00000514523.1:n.*580G>A
ENST00000699685.1:n.1191G>A
ENST00000699686.1:c.780G>A	ENSP00000514524.1:p.Lys260=
ENST00000699687.1:c.882G>A	ENSP00000514525.1:p.Lys294=
ENST00000699688.1:n.1187G>A
ENST00000699689.1:n.1543G>A
ENST00000699690.1:n.1740G>A
ENST00000699691.1:n.1884G>A
ENST00000699693.1:n.1404G>A
ENST00000699694.1:n.1646G>A
ENST00000699695.1:c.*359G>A	ENSP00000514526.1:n.*359G>A
ENST00000699696.1:n.1290G>A
ENST00000699697.1:c.987G>A	ENSP00000514527.1:p.Lys329=
ENST00000699698.1:n.908G>A
ENST00000699699.1:n.1311G>A
ENST00000699700.1:n.1434G>A
ENST00000699701.1:c.*367G>A	ENSP00000514528.1:n.*367G>A
ENST00000267415.12:c.987G>A MANE Select	ENSP00000267415.7:p.Lys329=
ENST00000646753.1:c.882G>A	ENSP00000494065.1:p.Lys294=
ENST00000267415.11:c.987G>A	ENSP00000267415.7:p.Lys329=
ENST00000399423.8:c.987G>A	ENSP00000382350.4:p.Lys329=
ENST00000557915.1:n.106G>A
ENST00000558566.1:c.*359G>A	ENSP00000453025.1:n.*359G>A
ENST00000559019.1:c.*359G>A	ENSP00000453675.1:n.*359G>A
ENST00000559969.5:c.758-13G>A
ENST00000626689.2:c.*359G>A	ENSP00000486681.1:n.*359G>A
NM_001099274.1:c.987G>A	NP_001092744.1:p.Lys329=
NM_012461.2:c.987G>A	NP_036593.2:p.Lys329=
XM_005267528.2:c.987G>A	XP_005267585.1:p.Lys329=
XM_005267529.2:c.882G>A	XP_005267586.1:p.Lys294=
NM_001099274.2:c.987G>A	NP_001092744.1:p.Lys329=
NM_001363668.1:c.882G>A	NP_001350597.1:p.Lys294=
NM_012461.3:c.987G>A	NP_036593.2:p.Lys329=
XM_011536642.2:c.*367G>A	XP_011534944.1:n.*367G>A
XM_017021216.2:c.345G>A	XP_016876705.1:p.Lys115=
XM_017021217.1:c.345G>A	XP_016876706.1:p.Lys115=
NM_001099274.3:c.987G>A MANE Select	NP_001092744.1:p.Lys329=
NM_001363668.2:c.882G>A	NP_001350597.1:p.Lys294=