Canonical Allele Identifier: CA389224727

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709763T>A (hg19) ; chr14:g.24240557T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240557T>A , CM000676.2:g.24240557T>A	GRCh38
NC_000014.8:g.24709763T>A , CM000676.1:g.24709763T>A	GRCh37
NC_000014.7:g.23779603T>A	NCBI36
NG_016650.1:g.7118A>T
NG_054634.1:g.13141T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1226A>T
ENST00000557921.3:c.815A>T	ENSP00000453157.3:p.Glu272Val
ENST00000699682.1:n.1313A>T
ENST00000699683.1:n.1363A>T
ENST00000699684.1:c.*516A>T	ENSP00000514523.1:n.*516A>T
ENST00000699685.1:n.1127A>T
ENST00000699686.1:c.716A>T	ENSP00000514524.1:p.Glu239Val
ENST00000699687.1:c.818A>T	ENSP00000514525.1:p.Glu273Val
ENST00000699688.1:n.1123A>T
ENST00000699689.1:n.1479A>T
ENST00000699690.1:n.1676A>T
ENST00000699691.1:n.1820A>T
ENST00000699693.1:n.1340A>T
ENST00000699694.1:n.1582A>T
ENST00000699695.1:c.*295A>T	ENSP00000514526.1:n.*295A>T
ENST00000699696.1:n.1226A>T
ENST00000699697.1:c.923A>T	ENSP00000514527.1:p.Glu308Val
ENST00000699698.1:n.844A>T
ENST00000699699.1:n.1247A>T
ENST00000699700.1:n.1370A>T
ENST00000699701.1:c.*303A>T	ENSP00000514528.1:n.*303A>T
ENST00000267415.12:c.923A>T MANE Select	ENSP00000267415.7:p.Glu308Val
ENST00000557921.2:c.815A>T	ENSP00000453157.2:p.Glu272Val
ENST00000646753.1:c.818A>T	ENSP00000494065.1:p.Glu273Val
ENST00000267415.11:c.923A>T	ENSP00000267415.7:p.Glu308Val
ENST00000399423.8:c.923A>T	ENSP00000382350.4:p.Glu308Val
ENST00000557915.1:n.42A>T
ENST00000558566.1:c.*295A>T	ENSP00000453025.1:n.*295A>T
ENST00000559019.1:c.*295A>T	ENSP00000453675.1:n.*295A>T
ENST00000559969.5:c.758-77A>T
ENST00000626689.2:c.*295A>T	ENSP00000486681.1:n.*295A>T
NM_001099274.1:c.923A>T	NP_001092744.1:p.Glu308Val
NM_012461.2:c.923A>T	NP_036593.2:p.Glu308Val
XM_005267528.2:c.923A>T	XP_005267585.1:p.Glu308Val
XM_005267529.2:c.818A>T	XP_005267586.1:p.Glu273Val
NM_001099274.2:c.923A>T	NP_001092744.1:p.Glu308Val
NM_001363668.1:c.818A>T	NP_001350597.1:p.Glu273Val
NM_012461.3:c.923A>T	NP_036593.2:p.Glu308Val
XM_011536642.2:c.*303A>T	XP_011534944.1:n.*303A>T
XM_017021216.2:c.281A>T	XP_016876705.1:p.Glu94Val
XM_017021217.1:c.281A>T	XP_016876706.1:p.Glu94Val
NM_001099274.3:c.923A>T MANE Select	NP_001092744.1:p.Glu308Val
NM_001363668.2:c.818A>T	NP_001350597.1:p.Glu273Val