Canonical Allele Identifier: CA2123849358

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240746G= , CM000676.2:g.24240746G=	GRCh38
NC_000014.8:g.24709952G= , CM000676.1:g.24709952G=	GRCh37
NC_000014.7:g.23779792G=	NCBI36
NG_016650.1:g.6929C=
NG_054634.1:g.13330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1037C=
ENST00000557921.3:c.626C=	ENSP00000453157.3:p.Ser209=
ENST00000699682.1:n.1124C=
ENST00000699683.1:n.1174C=
ENST00000699684.1:c.*327C=	ENSP00000514523.1:n.*327C=
ENST00000699685.1:n.938C=
ENST00000699686.1:c.527C=	ENSP00000514524.1:p.Ser176=
ENST00000699687.1:c.629C=	ENSP00000514525.1:p.Ser210=
ENST00000699688.1:n.934C=
ENST00000699689.1:n.1290C=
ENST00000699690.1:n.1487C=
ENST00000699691.1:n.1631C=
ENST00000699693.1:n.1151C=
ENST00000699694.1:n.1393C=
ENST00000699695.1:c.*106C=	ENSP00000514526.1:n.*106C=
ENST00000699696.1:n.1037C=
ENST00000699697.1:c.734C=	ENSP00000514527.1:p.Ser245=
ENST00000699698.1:n.655C=
ENST00000699699.1:n.1058C=
ENST00000699700.1:n.1181C=
ENST00000699701.1:c.*114C=	ENSP00000514528.1:n.*114C=
ENST00000267415.12:c.734C= MANE Select	ENSP00000267415.7:p.Ser245=
ENST00000557921.2:c.626C=	ENSP00000453157.2:p.Ser209=
ENST00000646753.1:c.629C=	ENSP00000494065.1:p.Ser210=
ENST00000267415.11:c.734C=	ENSP00000267415.7:p.Ser245=
ENST00000399423.8:c.734C=	ENSP00000382350.4:p.Ser245=
ENST00000558476.5:c.296C=	ENSP00000452724.1:p.Ser99=
ENST00000558566.1:c.*106C=	ENSP00000453025.1:n.*106C=
ENST00000559019.1:c.*106C=	ENSP00000453675.1:n.*106C=
ENST00000559549.1:n.460C=
ENST00000559969.5:c.690C=
ENST00000626689.2:c.*106C=	ENSP00000486681.1:n.*106C=
NM_001099274.1:c.734C=	NP_001092744.1:p.Ser245=
NM_012461.2:c.734C=	NP_036593.2:p.Ser245=
XM_005267528.2:c.734C=	XP_005267585.1:p.Ser245=
XM_005267529.2:c.629C=	XP_005267586.1:p.Ser210=
NM_001099274.2:c.734C=	NP_001092744.1:p.Ser245=
NM_001363668.1:c.629C=	NP_001350597.1:p.Ser210=
NM_012461.3:c.734C=	NP_036593.2:p.Ser245=
XM_011536642.2:c.*114C=	XP_011534944.1:n.*114C=
XM_017021216.2:c.92C=	XP_016876705.1:p.Ser31=
XM_017021217.1:c.92C=	XP_016876706.1:p.Ser31=
NM_001099274.3:c.734C= MANE Select	NP_001092744.1:p.Ser245=
NM_001363668.2:c.629C=	NP_001350597.1:p.Ser210=