Canonical Allele Identifier: CA389223828

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709687C>A (hg19) ; chr14:g.24240481C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240481C>A , CM000676.2:g.24240481C>A	GRCh38
NC_000014.8:g.24709687C>A , CM000676.1:g.24709687C>A	GRCh37
NC_000014.7:g.23779527C>A	NCBI36
NG_016650.1:g.7194G>T
NG_054634.1:g.13065C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1302G>T
ENST00000557921.3:c.891G>T	ENSP00000453157.3:p.Gln297His
ENST00000699682.1:n.1389G>T
ENST00000699683.1:n.1439G>T
ENST00000699684.1:c.*592G>T	ENSP00000514523.1:n.*592G>T
ENST00000699685.1:n.1203G>T
ENST00000699686.1:c.792G>T	ENSP00000514524.1:p.Gln264His
ENST00000699687.1:c.894G>T	ENSP00000514525.1:p.Gln298His
ENST00000699688.1:n.1199G>T
ENST00000699689.1:n.1555G>T
ENST00000699690.1:n.1752G>T
ENST00000699691.1:n.1896G>T
ENST00000699693.1:n.1416G>T
ENST00000699694.1:n.1658G>T
ENST00000699695.1:c.*371G>T	ENSP00000514526.1:n.*371G>T
ENST00000699696.1:n.1302G>T
ENST00000699697.1:c.999G>T	ENSP00000514527.1:p.Gln333His
ENST00000699698.1:n.920G>T
ENST00000699699.1:n.1323G>T
ENST00000699700.1:n.1446G>T
ENST00000699701.1:c.*379G>T	ENSP00000514528.1:n.*379G>T
ENST00000267415.12:c.999G>T MANE Select	ENSP00000267415.7:p.Gln333His
ENST00000646753.1:c.894G>T	ENSP00000494065.1:p.Gln298His
ENST00000267415.11:c.999G>T	ENSP00000267415.7:p.Gln333His
ENST00000399423.8:c.999G>T	ENSP00000382350.4:p.Gln333His
ENST00000557915.1:n.118G>T
ENST00000558566.1:c.*371G>T	ENSP00000453025.1:n.*371G>T
ENST00000559969.5:c.758-1G>T
ENST00000626689.2:c.*371G>T	ENSP00000486681.1:n.*371G>T
NM_001099274.1:c.999G>T	NP_001092744.1:p.Gln333His
NM_012461.2:c.999G>T	NP_036593.2:p.Gln333His
XM_005267528.2:c.999G>T	XP_005267585.1:p.Gln333His
XM_005267529.2:c.894G>T	XP_005267586.1:p.Gln298His
NM_001099274.2:c.999G>T	NP_001092744.1:p.Gln333His
NM_001363668.1:c.894G>T	NP_001350597.1:p.Gln298His
NM_012461.3:c.999G>T	NP_036593.2:p.Gln333His
XM_011536642.2:c.*379G>T	XP_011534944.1:n.*379G>T
XM_017021216.2:c.357G>T	XP_016876705.1:p.Gln119His
XM_017021217.1:c.357G>T	XP_016876706.1:p.Gln119His
NM_001099274.3:c.999G>T MANE Select	NP_001092744.1:p.Gln333His
NM_001363668.2:c.894G>T	NP_001350597.1:p.Gln298His