Canonical Allele Identifier: CA2123849275

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240567T= , CM000676.2:g.24240567T=	GRCh38
NC_000014.8:g.24709773T= , CM000676.1:g.24709773T=	GRCh37
NC_000014.7:g.23779613T=	NCBI36
NG_016650.1:g.7108A=
NG_054634.1:g.13151T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1216A=
ENST00000557921.3:c.805A=	ENSP00000453157.3:p.Ser269=
ENST00000699682.1:n.1303A=
ENST00000699683.1:n.1353A=
ENST00000699684.1:c.*506A=	ENSP00000514523.1:n.*506A=
ENST00000699685.1:n.1117A=
ENST00000699686.1:c.706A=	ENSP00000514524.1:p.Ser236=
ENST00000699687.1:c.808A=	ENSP00000514525.1:p.Ser270=
ENST00000699688.1:n.1113A=
ENST00000699689.1:n.1469A=
ENST00000699690.1:n.1666A=
ENST00000699691.1:n.1810A=
ENST00000699693.1:n.1330A=
ENST00000699694.1:n.1572A=
ENST00000699695.1:c.*285A=	ENSP00000514526.1:n.*285A=
ENST00000699696.1:n.1216A=
ENST00000699697.1:c.913A=	ENSP00000514527.1:p.Ser305=
ENST00000699698.1:n.834A=
ENST00000699699.1:n.1237A=
ENST00000699700.1:n.1360A=
ENST00000699701.1:c.*293A=	ENSP00000514528.1:n.*293A=
ENST00000267415.12:c.913A= MANE Select	ENSP00000267415.7:p.Ser305=
ENST00000557921.2:c.805A=	ENSP00000453157.2:p.Ser269=
ENST00000646753.1:c.808A=	ENSP00000494065.1:p.Ser270=
ENST00000267415.11:c.913A=	ENSP00000267415.7:p.Ser305=
ENST00000399423.8:c.913A=	ENSP00000382350.4:p.Ser305=
ENST00000557915.1:n.32A=
ENST00000558566.1:c.*285A=	ENSP00000453025.1:n.*285A=
ENST00000559019.1:c.*285A=	ENSP00000453675.1:n.*285A=
ENST00000559969.5:c.758-87A=
ENST00000626689.2:c.*285A=	ENSP00000486681.1:n.*285A=
NM_001099274.1:c.913A=	NP_001092744.1:p.Ser305=
NM_012461.2:c.913A=	NP_036593.2:p.Ser305=
XM_005267528.2:c.913A=	XP_005267585.1:p.Ser305=
XM_005267529.2:c.808A=	XP_005267586.1:p.Ser270=
NM_001099274.2:c.913A=	NP_001092744.1:p.Ser305=
NM_001363668.1:c.808A=	NP_001350597.1:p.Ser270=
NM_012461.3:c.913A=	NP_036593.2:p.Ser305=
XM_011536642.2:c.*293A=	XP_011534944.1:n.*293A=
XM_017021216.2:c.271A=	XP_016876705.1:p.Ser91=
XM_017021217.1:c.271A=	XP_016876706.1:p.Ser91=
NM_001099274.3:c.913A= MANE Select	NP_001092744.1:p.Ser305=
NM_001363668.2:c.808A=	NP_001350597.1:p.Ser270=