Canonical Allele Identifier: CA389226564

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240717C>G , CM000676.2:g.24240717C>G	GRCh38
NC_000014.8:g.24709923C>G , CM000676.1:g.24709923C>G	GRCh37
NC_000014.7:g.23779763C>G	NCBI36
NG_016650.1:g.6958G>C
NG_054634.1:g.13301C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1066G>C
ENST00000557921.3:c.655G>C	ENSP00000453157.3:p.Gly219Arg
ENST00000699682.1:n.1153G>C
ENST00000699683.1:n.1203G>C
ENST00000699684.1:c.*356G>C	ENSP00000514523.1:n.*356G>C
ENST00000699685.1:n.967G>C
ENST00000699686.1:c.556G>C	ENSP00000514524.1:p.Gly186Arg
ENST00000699687.1:c.658G>C	ENSP00000514525.1:p.Gly220Arg
ENST00000699688.1:n.963G>C
ENST00000699689.1:n.1319G>C
ENST00000699690.1:n.1516G>C
ENST00000699691.1:n.1660G>C
ENST00000699693.1:n.1180G>C
ENST00000699694.1:n.1422G>C
ENST00000699695.1:c.*135G>C	ENSP00000514526.1:n.*135G>C
ENST00000699696.1:n.1066G>C
ENST00000699697.1:c.763G>C	ENSP00000514527.1:p.Gly255Arg
ENST00000699698.1:n.684G>C
ENST00000699699.1:n.1087G>C
ENST00000699700.1:n.1210G>C
ENST00000699701.1:c.*143G>C	ENSP00000514528.1:n.*143G>C
ENST00000267415.12:c.763G>C MANE Select	ENSP00000267415.7:p.Gly255Arg
ENST00000557921.2:c.655G>C	ENSP00000453157.2:p.Gly219Arg
ENST00000646753.1:c.658G>C	ENSP00000494065.1:p.Gly220Arg
ENST00000267415.11:c.763G>C	ENSP00000267415.7:p.Gly255Arg
ENST00000399423.8:c.763G>C	ENSP00000382350.4:p.Gly255Arg
ENST00000558476.5:c.325G>C	ENSP00000452724.1:p.Gly109Arg
ENST00000558566.1:c.*135G>C	ENSP00000453025.1:n.*135G>C
ENST00000559019.1:c.*135G>C	ENSP00000453675.1:n.*135G>C
ENST00000559549.1:n.489G>C
ENST00000559969.5:c.719G>C
ENST00000626689.2:c.*135G>C	ENSP00000486681.1:n.*135G>C
NM_001099274.1:c.763G>C	NP_001092744.1:p.Gly255Arg
NM_012461.2:c.763G>C	NP_036593.2:p.Gly255Arg
XM_005267528.2:c.763G>C	XP_005267585.1:p.Gly255Arg
XM_005267529.2:c.658G>C	XP_005267586.1:p.Gly220Arg
NM_001099274.2:c.763G>C	NP_001092744.1:p.Gly255Arg
NM_001363668.1:c.658G>C	NP_001350597.1:p.Gly220Arg
NM_012461.3:c.763G>C	NP_036593.2:p.Gly255Arg
XM_011536642.2:c.*143G>C	XP_011534944.1:n.*143G>C
XM_017021216.2:c.121G>C	XP_016876705.1:p.Gly41Arg
XM_017021217.1:c.121G>C	XP_016876706.1:p.Gly41Arg
NM_001099274.3:c.763G>C MANE Select	NP_001092744.1:p.Gly255Arg
NM_001363668.2:c.658G>C	NP_001350597.1:p.Gly220Arg