Canonical Allele Identifier: CA389225182

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709805C>T (hg19) ; chr14:g.24240599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240599C>T , CM000676.2:g.24240599C>T	GRCh38
NC_000014.8:g.24709805C>T , CM000676.1:g.24709805C>T	GRCh37
NC_000014.7:g.23779645C>T	NCBI36
NG_016650.1:g.7076G>A
NG_054634.1:g.13183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1184G>A
ENST00000557921.3:c.773G>A	ENSP00000453157.3:p.Gly258Asp
ENST00000699682.1:n.1271G>A
ENST00000699683.1:n.1321G>A
ENST00000699684.1:c.*474G>A	ENSP00000514523.1:n.*474G>A
ENST00000699685.1:n.1085G>A
ENST00000699686.1:c.674G>A	ENSP00000514524.1:p.Gly225Asp
ENST00000699687.1:c.776G>A	ENSP00000514525.1:p.Gly259Asp
ENST00000699688.1:n.1081G>A
ENST00000699689.1:n.1437G>A
ENST00000699690.1:n.1634G>A
ENST00000699691.1:n.1778G>A
ENST00000699693.1:n.1298G>A
ENST00000699694.1:n.1540G>A
ENST00000699695.1:c.*253G>A	ENSP00000514526.1:n.*253G>A
ENST00000699696.1:n.1184G>A
ENST00000699697.1:c.881G>A	ENSP00000514527.1:p.Gly294Asp
ENST00000699698.1:n.802G>A
ENST00000699699.1:n.1205G>A
ENST00000699700.1:n.1328G>A
ENST00000699701.1:c.*261G>A	ENSP00000514528.1:n.*261G>A
ENST00000267415.12:c.881G>A MANE Select	ENSP00000267415.7:p.Gly294Asp
ENST00000557921.2:c.773G>A	ENSP00000453157.2:p.Gly258Asp
ENST00000646753.1:c.776G>A	ENSP00000494065.1:p.Gly259Asp
ENST00000267415.11:c.881G>A	ENSP00000267415.7:p.Gly294Asp
ENST00000399423.8:c.881G>A	ENSP00000382350.4:p.Gly294Asp
ENST00000558566.1:c.*253G>A	ENSP00000453025.1:n.*253G>A
ENST00000559019.1:c.*253G>A	ENSP00000453675.1:n.*253G>A
ENST00000559549.1:n.607G>A
ENST00000559969.5:c.757+80G>A
ENST00000626689.2:c.*253G>A	ENSP00000486681.1:n.*253G>A
NM_001099274.1:c.881G>A	NP_001092744.1:p.Gly294Asp
NM_012461.2:c.881G>A	NP_036593.2:p.Gly294Asp
XM_005267528.2:c.881G>A	XP_005267585.1:p.Gly294Asp
XM_005267529.2:c.776G>A	XP_005267586.1:p.Gly259Asp
NM_001099274.2:c.881G>A	NP_001092744.1:p.Gly294Asp
NM_001363668.1:c.776G>A	NP_001350597.1:p.Gly259Asp
NM_012461.3:c.881G>A	NP_036593.2:p.Gly294Asp
XM_011536642.2:c.*261G>A	XP_011534944.1:n.*261G>A
XM_017021216.2:c.239G>A	XP_016876705.1:p.Gly80Asp
XM_017021217.1:c.239G>A	XP_016876706.1:p.Gly80Asp
NM_001099274.3:c.881G>A MANE Select	NP_001092744.1:p.Gly294Asp
NM_001363668.2:c.776G>A	NP_001350597.1:p.Gly259Asp