Canonical Allele Identifier: CA389224073

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709710C>G (hg19) ; chr14:g.24240504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240504C>G , CM000676.2:g.24240504C>G	GRCh38
NC_000014.8:g.24709710C>G , CM000676.1:g.24709710C>G	GRCh37
NC_000014.7:g.23779550C>G	NCBI36
NG_016650.1:g.7171G>C
NG_054634.1:g.13088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1279G>C
ENST00000557921.3:c.868G>C	ENSP00000453157.3:p.Gly290Arg
ENST00000699682.1:n.1366G>C
ENST00000699683.1:n.1416G>C
ENST00000699684.1:c.*569G>C	ENSP00000514523.1:n.*569G>C
ENST00000699685.1:n.1180G>C
ENST00000699686.1:c.769G>C	ENSP00000514524.1:p.Gly257Arg
ENST00000699687.1:c.871G>C	ENSP00000514525.1:p.Gly291Arg
ENST00000699688.1:n.1176G>C
ENST00000699689.1:n.1532G>C
ENST00000699690.1:n.1729G>C
ENST00000699691.1:n.1873G>C
ENST00000699693.1:n.1393G>C
ENST00000699694.1:n.1635G>C
ENST00000699695.1:c.*348G>C	ENSP00000514526.1:n.*348G>C
ENST00000699696.1:n.1279G>C
ENST00000699697.1:c.976G>C	ENSP00000514527.1:p.Gly326Arg
ENST00000699698.1:n.897G>C
ENST00000699699.1:n.1300G>C
ENST00000699700.1:n.1423G>C
ENST00000699701.1:c.*356G>C	ENSP00000514528.1:n.*356G>C
ENST00000267415.12:c.976G>C MANE Select	ENSP00000267415.7:p.Gly326Arg
ENST00000557921.2:c.868G>C	ENSP00000453157.2:p.Gly290Arg
ENST00000646753.1:c.871G>C	ENSP00000494065.1:p.Gly291Arg
ENST00000267415.11:c.976G>C	ENSP00000267415.7:p.Gly326Arg
ENST00000399423.8:c.976G>C	ENSP00000382350.4:p.Gly326Arg
ENST00000557915.1:n.95G>C
ENST00000558566.1:c.*348G>C	ENSP00000453025.1:n.*348G>C
ENST00000559019.1:c.*348G>C	ENSP00000453675.1:n.*348G>C
ENST00000559969.5:c.758-24G>C
ENST00000626689.2:c.*348G>C	ENSP00000486681.1:n.*348G>C
NM_001099274.1:c.976G>C	NP_001092744.1:p.Gly326Arg
NM_012461.2:c.976G>C	NP_036593.2:p.Gly326Arg
XM_005267528.2:c.976G>C	XP_005267585.1:p.Gly326Arg
XM_005267529.2:c.871G>C	XP_005267586.1:p.Gly291Arg
NM_001099274.2:c.976G>C	NP_001092744.1:p.Gly326Arg
NM_001363668.1:c.871G>C	NP_001350597.1:p.Gly291Arg
NM_012461.3:c.976G>C	NP_036593.2:p.Gly326Arg
XM_011536642.2:c.*356G>C	XP_011534944.1:n.*356G>C
XM_017021216.2:c.334G>C	XP_016876705.1:p.Gly112Arg
XM_017021217.1:c.334G>C	XP_016876706.1:p.Gly112Arg
NM_001099274.3:c.976G>C MANE Select	NP_001092744.1:p.Gly326Arg
NM_001363668.2:c.871G>C	NP_001350597.1:p.Gly291Arg