Canonical Allele Identifier: CA2123849260

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240543T= , CM000676.2:g.24240543T=	GRCh38
NC_000014.8:g.24709749T= , CM000676.1:g.24709749T=	GRCh37
NC_000014.7:g.23779589T=	NCBI36
NG_016650.1:g.7132A=
NG_054634.1:g.13127T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1240A=
ENST00000557921.3:c.829A=	ENSP00000453157.3:p.Thr277=
ENST00000699682.1:n.1327A=
ENST00000699683.1:n.1377A=
ENST00000699684.1:c.*530A=	ENSP00000514523.1:n.*530A=
ENST00000699685.1:n.1141A=
ENST00000699686.1:c.730A=	ENSP00000514524.1:p.Thr244=
ENST00000699687.1:c.832A=	ENSP00000514525.1:p.Thr278=
ENST00000699688.1:n.1137A=
ENST00000699689.1:n.1493A=
ENST00000699690.1:n.1690A=
ENST00000699691.1:n.1834A=
ENST00000699693.1:n.1354A=
ENST00000699694.1:n.1596A=
ENST00000699695.1:c.*309A=	ENSP00000514526.1:n.*309A=
ENST00000699696.1:n.1240A=
ENST00000699697.1:c.937A=	ENSP00000514527.1:p.Thr313=
ENST00000699698.1:n.858A=
ENST00000699699.1:n.1261A=
ENST00000699700.1:n.1384A=
ENST00000699701.1:c.*317A=	ENSP00000514528.1:n.*317A=
ENST00000267415.12:c.937A= MANE Select	ENSP00000267415.7:p.Thr313=
ENST00000557921.2:c.829A=	ENSP00000453157.2:p.Thr277=
ENST00000646753.1:c.832A=	ENSP00000494065.1:p.Thr278=
ENST00000267415.11:c.937A=	ENSP00000267415.7:p.Thr313=
ENST00000399423.8:c.937A=	ENSP00000382350.4:p.Thr313=
ENST00000557915.1:n.56A=
ENST00000558566.1:c.*309A=	ENSP00000453025.1:n.*309A=
ENST00000559019.1:c.*309A=	ENSP00000453675.1:n.*309A=
ENST00000559969.5:c.758-63A=
ENST00000626689.2:c.*309A=	ENSP00000486681.1:n.*309A=
NM_001099274.1:c.937A=	NP_001092744.1:p.Thr313=
NM_012461.2:c.937A=	NP_036593.2:p.Thr313=
XM_005267528.2:c.937A=	XP_005267585.1:p.Thr313=
XM_005267529.2:c.832A=	XP_005267586.1:p.Thr278=
NM_001099274.2:c.937A=	NP_001092744.1:p.Thr313=
NM_001363668.1:c.832A=	NP_001350597.1:p.Thr278=
NM_012461.3:c.937A=	NP_036593.2:p.Thr313=
XM_011536642.2:c.*317A=	XP_011534944.1:n.*317A=
XM_017021216.2:c.295A=	XP_016876705.1:p.Thr99=
XM_017021217.1:c.295A=	XP_016876706.1:p.Thr99=
NM_001099274.3:c.937A= MANE Select	NP_001092744.1:p.Thr313=
NM_001363668.2:c.832A=	NP_001350597.1:p.Thr278=