Canonical Allele Identifier: CA2123849306

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240639C= , CM000676.2:g.24240639C=	GRCh38
NC_000014.8:g.24709845C= , CM000676.1:g.24709845C=	GRCh37
NC_000014.7:g.23779685C=	NCBI36
NG_016650.1:g.7036G=
NG_054634.1:g.13223C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001099274.3:c.841G= MANE Select	NP_001092744.1:p.Glu281=
ENST00000267415.12:c.841G= MANE Select	ENSP00000267415.7:p.Glu281=
NM_001099274.1:c.841G=	NP_001092744.1:p.Glu281=
NM_001099274.2:c.841G=	NP_001092744.1:p.Glu281=
NM_001363668.1:c.736G=	NP_001350597.1:p.Glu246=
NM_001363668.2:c.736G=	NP_001350597.1:p.Glu246=
NM_012461.2:c.841G=	NP_036593.2:p.Glu281=
NM_012461.3:c.841G=	NP_036593.2:p.Glu281=
ENST00000267415.11:c.841G=	ENSP00000267415.7:p.Glu281=
ENST00000399423.8:c.841G=	ENSP00000382350.4:p.Glu281=
ENST00000557915.2:n.1144G=
ENST00000557921.2:c.733G=	ENSP00000453157.2:p.Glu245=
ENST00000557921.3:c.733G=	ENSP00000453157.3:p.Glu245=
ENST00000558476.5:c.403G=	ENSP00000452724.1:p.Glu135=
ENST00000558566.1:c.*213G=	ENSP00000453025.1:n.*213G=
ENST00000559019.1:c.*213G=	ENSP00000453675.1:n.*213G=
ENST00000559549.1:n.567G=
ENST00000559969.5:c.757+40G=
ENST00000626689.2:c.*213G=	ENSP00000486681.1:n.*213G=
ENST00000646753.1:c.736G=	ENSP00000494065.1:p.Glu246=
ENST00000699682.1:n.1231G=
ENST00000699683.1:n.1281G=
ENST00000699684.1:c.*434G=	ENSP00000514523.1:n.*434G=
ENST00000699685.1:n.1045G=
ENST00000699686.1:c.634G=	ENSP00000514524.1:p.Glu212=
ENST00000699687.1:c.736G=	ENSP00000514525.1:p.Glu246=
ENST00000699688.1:n.1041G=
ENST00000699689.1:n.1397G=
ENST00000699690.1:n.1594G=
ENST00000699691.1:n.1738G=
ENST00000699693.1:n.1258G=
ENST00000699694.1:n.1500G=
ENST00000699695.1:c.*213G=	ENSP00000514526.1:n.*213G=
ENST00000699696.1:n.1144G=
ENST00000699697.1:c.841G=	ENSP00000514527.1:p.Glu281=
ENST00000699698.1:n.762G=
ENST00000699699.1:n.1165G=
ENST00000699700.1:n.1288G=
ENST00000699701.1:c.*221G=	ENSP00000514528.1:n.*221G=
XM_005267528.2:c.841G=	XP_005267585.1:p.Glu281=
XM_005267529.2:c.736G=	XP_005267586.1:p.Glu246=
XM_011536642.2:c.*221G=	XP_011534944.1:n.*221G=
XM_017021216.2:c.199G=	XP_016876705.1:p.Glu67=
XM_017021217.1:c.199G=	XP_016876706.1:p.Glu67=