Canonical Allele Identifier: CA919377172

Gene: TINF2

Linked Data

• dbSNP Id: rs869130378

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240213_24240214dup , CM000676.2:g.24240213_24240214dup	GRCh38
NC_000014.8:g.24709419_24709420dup , CM000676.1:g.24709419_24709420dup	GRCh37
NC_000014.7:g.23779259_23779260dup	NCBI36
NG_016650.1:g.7464_7465dup
NG_054634.1:g.12797_12798dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+52_1520+53dup
ENST00000557921.3:c.*204_*205dup	ENSP00000453157.3:n.*204_*205dup
ENST00000699682.1:n.1659_1660dup
ENST00000699683.1:n.1709_1710dup
ENST00000699684.1:c.*862_*863dup	ENSP00000514523.1:n.*862_*863dup
ENST00000699685.1:n.1473_1474dup
ENST00000699686.1:c.*204_*205dup	ENSP00000514524.1:n.*204_*205dup
ENST00000699687.1:c.*204_*205dup	ENSP00000514525.1:n.*204_*205dup
ENST00000699688.1:n.1469_1470dup
ENST00000699689.1:n.1825_1826dup
ENST00000699690.1:n.2022_2023dup
ENST00000699691.1:n.2166_2167dup
ENST00000699692.1:n.69-28_69-27dup
ENST00000699693.1:n.1546+52_1546+53dup
ENST00000699694.1:n.1928_1929dup
ENST00000699695.1:c.*501+52_*501+53dup	ENSP00000514526.1:n.*501+52_*501+53dup
ENST00000699696.1:n.1520+52_1520+53dup
ENST00000699697.1:c.*44_*45dup	ENSP00000514527.1:n.*44_*45dup
ENST00000699698.1:n.1102_1103dup
ENST00000699699.1:n.1593_1594dup
ENST00000699700.1:n.1716_1717dup
ENST00000699701.1:c.*649_*650dup	ENSP00000514528.1:n.*649_*650dup
ENST00000267415.12:c.1129+52_1129+53dup MANE Select	ENSP00000267415.7:n.1129+52_1129+53dup
ENST00000646753.1:c.1024+52_1024+53dup	ENSP00000494065.1:n.1024+52_1024+53dup
ENST00000267415.11:c.1129+52_1129+53dup	ENSP00000267415.7:n.1129+52_1129+53dup
ENST00000399423.8:c.*204_*205dup	ENSP00000382350.4:n.*204_*205dup
ENST00000557915.1:n.336+52_336+53dup
ENST00000558566.1:c.*641_*642dup	ENSP00000453025.1:n.*641_*642dup
ENST00000558703.1:n.32_33dup
ENST00000559969.5:c.1027_1028dup
ENST00000560019.5:c.124+52_124+53dup	ENSP00000453113.1:n.124+52_124+53dup
ENST00000626689.2:c.*501+52_*501+53dup	ENSP00000486681.1:n.*501+52_*501+53dup
NM_001099274.1:c.1129+52_1129+53dup	NP_001092744.1:n.1129+52_1129+53dup
NM_012461.2:c.*204_*205dup	NP_036593.2:n.*204_*205dup
XM_005267528.2:c.1129+52_1129+53dup	XP_005267585.1:n.1129+52_1129+53dup
XM_005267529.2:c.1024+52_1024+53dup	XP_005267586.1:n.1024+52_1024+53dup
NM_001099274.2:c.1129+52_1129+53dup	NP_001092744.1:n.1129+52_1129+53dup
NM_001363668.1:c.1024+52_1024+53dup	NP_001350597.1:n.1024+52_1024+53dup
NM_012461.3:c.*204_*205dup	NP_036593.2:n.*204_*205dup
XM_011536642.2:c.*649_*650dup	XP_011534944.1:n.*649_*650dup
XM_017021216.2:c.487+52_487+53dup	XP_016876705.1:n.487+52_487+53dup
XM_017021217.1:c.487+52_487+53dup	XP_016876706.1:n.487+52_487+53dup
NM_001099274.3:c.1129+52_1129+53dup MANE Select	NP_001092744.1:n.1129+52_1129+53dup
NM_001363668.2:c.1024+52_1024+53dup	NP_001350597.1:n.1024+52_1024+53dup