Canonical Allele Identifier: CA2123849292

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240618A= , CM000676.2:g.24240618A=	GRCh38
NC_000014.8:g.24709824A= , CM000676.1:g.24709824A=	GRCh37
NC_000014.7:g.23779664A=	NCBI36
NG_016650.1:g.7057T=
NG_054634.1:g.13202A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1165T=
ENST00000557921.3:c.754T=	ENSP00000453157.3:p.Phe252=
ENST00000699682.1:n.1252T=
ENST00000699683.1:n.1302T=
ENST00000699684.1:c.*455T=	ENSP00000514523.1:n.*455T=
ENST00000699685.1:n.1066T=
ENST00000699686.1:c.655T=	ENSP00000514524.1:p.Phe219=
ENST00000699687.1:c.757T=	ENSP00000514525.1:p.Phe253=
ENST00000699688.1:n.1062T=
ENST00000699689.1:n.1418T=
ENST00000699690.1:n.1615T=
ENST00000699691.1:n.1759T=
ENST00000699693.1:n.1279T=
ENST00000699694.1:n.1521T=
ENST00000699695.1:c.*234T=	ENSP00000514526.1:n.*234T=
ENST00000699696.1:n.1165T=
ENST00000699697.1:c.862T=	ENSP00000514527.1:p.Phe288=
ENST00000699698.1:n.783T=
ENST00000699699.1:n.1186T=
ENST00000699700.1:n.1309T=
ENST00000699701.1:c.*242T=	ENSP00000514528.1:n.*242T=
ENST00000267415.12:c.862T= MANE Select	ENSP00000267415.7:p.Phe288=
ENST00000557921.2:c.754T=	ENSP00000453157.2:p.Phe252=
ENST00000646753.1:c.757T=	ENSP00000494065.1:p.Phe253=
ENST00000267415.11:c.862T=	ENSP00000267415.7:p.Phe288=
ENST00000399423.8:c.862T=	ENSP00000382350.4:p.Phe288=
ENST00000558476.5:c.424T=	ENSP00000452724.1:p.Phe142=
ENST00000558566.1:c.*234T=	ENSP00000453025.1:n.*234T=
ENST00000559019.1:c.*234T=	ENSP00000453675.1:n.*234T=
ENST00000559549.1:n.588T=
ENST00000559969.5:c.757+61T=
ENST00000626689.2:c.*234T=	ENSP00000486681.1:n.*234T=
NM_001099274.1:c.862T=	NP_001092744.1:p.Phe288=
NM_012461.2:c.862T=	NP_036593.2:p.Phe288=
XM_005267528.2:c.862T=	XP_005267585.1:p.Phe288=
XM_005267529.2:c.757T=	XP_005267586.1:p.Phe253=
NM_001099274.2:c.862T=	NP_001092744.1:p.Phe288=
NM_001363668.1:c.757T=	NP_001350597.1:p.Phe253=
NM_012461.3:c.862T=	NP_036593.2:p.Phe288=
XM_011536642.2:c.*242T=	XP_011534944.1:n.*242T=
XM_017021216.2:c.220T=	XP_016876705.1:p.Phe74=
XM_017021217.1:c.220T=	XP_016876706.1:p.Phe74=
NM_001099274.3:c.862T= MANE Select	NP_001092744.1:p.Phe288=
NM_001363668.2:c.757T=	NP_001350597.1:p.Phe253=