Canonical Allele Identifier: CA2123849108

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240420C= , CM000676.2:g.24240420C=	GRCh38
NC_000014.8:g.24709626C= , CM000676.1:g.24709626C=	GRCh37
NC_000014.7:g.23779466C=	NCBI36
NG_016650.1:g.7255G=
NG_054634.1:g.13004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1363G=
ENST00000557921.3:c.952G=	ENSP00000453157.3:p.Glu318=
ENST00000699682.1:n.1450G=
ENST00000699683.1:n.1500G=
ENST00000699684.1:c.*653G=	ENSP00000514523.1:n.*653G=
ENST00000699685.1:n.1264G=
ENST00000699686.1:c.853G=	ENSP00000514524.1:p.Glu285=
ENST00000699687.1:c.955G=	ENSP00000514525.1:p.Glu319=
ENST00000699688.1:n.1260G=
ENST00000699689.1:n.1616G=
ENST00000699690.1:n.1813G=
ENST00000699691.1:n.1957G=
ENST00000699693.1:n.1477G=
ENST00000699694.1:n.1719G=
ENST00000699695.1:c.*432G=	ENSP00000514526.1:n.*432G=
ENST00000699696.1:n.1363G=
ENST00000699697.1:c.1060G=	ENSP00000514527.1:p.Glu354=
ENST00000699698.1:n.981G=
ENST00000699699.1:n.1384G=
ENST00000699700.1:n.1507G=
ENST00000699701.1:c.*440G=	ENSP00000514528.1:n.*440G=
ENST00000267415.12:c.1060G= MANE Select	ENSP00000267415.7:p.Glu354=
ENST00000646753.1:c.955G=	ENSP00000494065.1:p.Glu319=
ENST00000267415.11:c.1060G=	ENSP00000267415.7:p.Glu354=
ENST00000399423.8:c.1060G=	ENSP00000382350.4:p.Glu354=
ENST00000557915.1:n.179G=
ENST00000558566.1:c.*432G=	ENSP00000453025.1:n.*432G=
ENST00000559969.5:c.818G=
ENST00000560019.5:c.55G=	ENSP00000453113.1:p.Glu19=
ENST00000626689.2:c.*432G=	ENSP00000486681.1:n.*432G=
NM_001099274.1:c.1060G=	NP_001092744.1:p.Glu354=
NM_012461.2:c.1060G=	NP_036593.2:p.Glu354=
XM_005267528.2:c.1060G=	XP_005267585.1:p.Glu354=
XM_005267529.2:c.955G=	XP_005267586.1:p.Glu319=
NM_001099274.2:c.1060G=	NP_001092744.1:p.Glu354=
NM_001363668.1:c.955G=	NP_001350597.1:p.Glu319=
NM_012461.3:c.1060G=	NP_036593.2:p.Glu354=
XM_011536642.2:c.*440G=	XP_011534944.1:n.*440G=
XM_017021216.2:c.418G=	XP_016876705.1:p.Glu140=
XM_017021217.1:c.418G=	XP_016876706.1:p.Glu140=
NM_001099274.3:c.1060G= MANE Select	NP_001092744.1:p.Glu354=
NM_001363668.2:c.955G=	NP_001350597.1:p.Glu319=