Canonical Allele Identifier: CA257880909

Gene: TINF2

Linked Data

• dbSNP Id: rs776136324
• MyVariant Identifiers: chr14:g.24709774C>G (hg19) ; chr14:g.24240568C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240568C>G , CM000676.2:g.24240568C>G	GRCh38
NC_000014.8:g.24709774C>G , CM000676.1:g.24709774C>G	GRCh37
NC_000014.7:g.23779614C>G	NCBI36
NG_016650.1:g.7107G>C
NG_054634.1:g.13152C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1215G>C
ENST00000557921.3:c.804G>C	ENSP00000453157.3:p.Glu268Asp
ENST00000699682.1:n.1302G>C
ENST00000699683.1:n.1352G>C
ENST00000699684.1:c.*505G>C	ENSP00000514523.1:n.*505G>C
ENST00000699685.1:n.1116G>C
ENST00000699686.1:c.705G>C	ENSP00000514524.1:p.Glu235Asp
ENST00000699687.1:c.807G>C	ENSP00000514525.1:p.Glu269Asp
ENST00000699688.1:n.1112G>C
ENST00000699689.1:n.1468G>C
ENST00000699690.1:n.1665G>C
ENST00000699691.1:n.1809G>C
ENST00000699693.1:n.1329G>C
ENST00000699694.1:n.1571G>C
ENST00000699695.1:c.*284G>C	ENSP00000514526.1:n.*284G>C
ENST00000699696.1:n.1215G>C
ENST00000699697.1:c.912G>C	ENSP00000514527.1:p.Glu304Asp
ENST00000699698.1:n.833G>C
ENST00000699699.1:n.1236G>C
ENST00000699700.1:n.1359G>C
ENST00000699701.1:c.*292G>C	ENSP00000514528.1:n.*292G>C
ENST00000267415.12:c.912G>C MANE Select	ENSP00000267415.7:p.Glu304Asp
ENST00000557921.2:c.804G>C	ENSP00000453157.2:p.Glu268Asp
ENST00000646753.1:c.807G>C	ENSP00000494065.1:p.Glu269Asp
ENST00000267415.11:c.912G>C	ENSP00000267415.7:p.Glu304Asp
ENST00000399423.8:c.912G>C	ENSP00000382350.4:p.Glu304Asp
ENST00000557915.1:n.31G>C
ENST00000558566.1:c.*284G>C	ENSP00000453025.1:n.*284G>C
ENST00000559019.1:c.*284G>C	ENSP00000453675.1:n.*284G>C
ENST00000559969.5:c.758-88G>C
ENST00000626689.2:c.*284G>C	ENSP00000486681.1:n.*284G>C
NM_001099274.1:c.912G>C	NP_001092744.1:p.Glu304Asp
NM_012461.2:c.912G>C	NP_036593.2:p.Glu304Asp
XM_005267528.2:c.912G>C	XP_005267585.1:p.Glu304Asp
XM_005267529.2:c.807G>C	XP_005267586.1:p.Glu269Asp
NM_001099274.2:c.912G>C	NP_001092744.1:p.Glu304Asp
NM_001363668.1:c.807G>C	NP_001350597.1:p.Glu269Asp
NM_012461.3:c.912G>C	NP_036593.2:p.Glu304Asp
XM_011536642.2:c.*292G>C	XP_011534944.1:n.*292G>C
XM_017021216.2:c.270G>C	XP_016876705.1:p.Glu90Asp
XM_017021217.1:c.270G>C	XP_016876706.1:p.Glu90Asp
NM_001099274.3:c.912G>C MANE Select	NP_001092744.1:p.Glu304Asp
NM_001363668.2:c.807G>C	NP_001350597.1:p.Glu269Asp