Canonical Allele Identifier: CA389222379

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709468C>T (hg19) ; chr14:g.24240262C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240262C>T , CM000676.2:g.24240262C>T	GRCh38
NC_000014.8:g.24709468C>T , CM000676.1:g.24709468C>T	GRCh37
NC_000014.7:g.23779308C>T	NCBI36
NG_016650.1:g.7413G>A
NG_054634.1:g.12846C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+1G>A
ENST00000557921.3:c.*153G>A	ENSP00000453157.3:n.*153G>A
ENST00000699682.1:n.1608G>A
ENST00000699683.1:n.1658G>A
ENST00000699684.1:c.*811G>A	ENSP00000514523.1:n.*811G>A
ENST00000699685.1:n.1422G>A
ENST00000699686.1:c.*153G>A	ENSP00000514524.1:n.*153G>A
ENST00000699687.1:c.*153G>A	ENSP00000514525.1:n.*153G>A
ENST00000699688.1:n.1418G>A
ENST00000699689.1:n.1774G>A
ENST00000699690.1:n.1971G>A
ENST00000699691.1:n.2115G>A
ENST00000699692.1:n.68+1G>A
ENST00000699693.1:n.1546+1G>A
ENST00000699694.1:n.1877G>A
ENST00000699695.1:c.*501+1G>A	ENSP00000514526.1:n.*501+1G>A
ENST00000699696.1:n.1520+1G>A
ENST00000699697.1:c.1130G>A	ENSP00000514527.1:p.Gly377Asp
ENST00000699698.1:n.1051G>A
ENST00000699699.1:n.1542G>A
ENST00000699700.1:n.1665G>A
ENST00000699701.1:c.*598G>A	ENSP00000514528.1:n.*598G>A
ENST00000267415.12:c.1129+1G>A MANE Select	ENSP00000267415.7:n.1129+1G>A
ENST00000646753.1:c.1024+1G>A	ENSP00000494065.1:n.1024+1G>A
ENST00000267415.11:c.1129+1G>A	ENSP00000267415.7:n.1129+1G>A
ENST00000399423.8:c.*153G>A	ENSP00000382350.4:n.*153G>A
ENST00000557915.1:n.336+1G>A
ENST00000558566.1:c.*590G>A	ENSP00000453025.1:n.*590G>A
ENST00000559969.5:c.976G>A
ENST00000560019.5:c.124+1G>A	ENSP00000453113.1:n.124+1G>A
ENST00000626689.2:c.*501+1G>A	ENSP00000486681.1:n.*501+1G>A
NM_001099274.1:c.1129+1G>A	NP_001092744.1:n.1129+1G>A
NM_012461.2:c.*153G>A	NP_036593.2:n.*153G>A
XM_005267528.2:c.1129+1G>A	XP_005267585.1:n.1129+1G>A
XM_005267529.2:c.1024+1G>A	XP_005267586.1:n.1024+1G>A
NM_001099274.2:c.1129+1G>A	NP_001092744.1:n.1129+1G>A
NM_001363668.1:c.1024+1G>A	NP_001350597.1:n.1024+1G>A
NM_012461.3:c.*153G>A	NP_036593.2:n.*153G>A
XM_011536642.2:c.*598G>A	XP_011534944.1:n.*598G>A
XM_017021216.2:c.487+1G>A	XP_016876705.1:n.487+1G>A
XM_017021217.1:c.487+1G>A	XP_016876706.1:n.487+1G>A
NM_001099274.3:c.1129+1G>A MANE Select	NP_001092744.1:n.1129+1G>A
NM_001363668.2:c.1024+1G>A	NP_001350597.1:n.1024+1G>A