Canonical Allele Identifier: CA2123849344

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240715G= , CM000676.2:g.24240715G=	GRCh38
NC_000014.8:g.24709921G= , CM000676.1:g.24709921G=	GRCh37
NC_000014.7:g.23779761G=	NCBI36
NG_016650.1:g.6960C=
NG_054634.1:g.13299G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1068C=
ENST00000557921.3:c.657C=	ENSP00000453157.3:p.Gly219=
ENST00000699682.1:n.1155C=
ENST00000699683.1:n.1205C=
ENST00000699684.1:c.*358C=	ENSP00000514523.1:n.*358C=
ENST00000699685.1:n.969C=
ENST00000699686.1:c.558C=	ENSP00000514524.1:p.Gly186=
ENST00000699687.1:c.660C=	ENSP00000514525.1:p.Gly220=
ENST00000699688.1:n.965C=
ENST00000699689.1:n.1321C=
ENST00000699690.1:n.1518C=
ENST00000699691.1:n.1662C=
ENST00000699693.1:n.1182C=
ENST00000699694.1:n.1424C=
ENST00000699695.1:c.*137C=	ENSP00000514526.1:n.*137C=
ENST00000699696.1:n.1068C=
ENST00000699697.1:c.765C=	ENSP00000514527.1:p.Gly255=
ENST00000699698.1:n.686C=
ENST00000699699.1:n.1089C=
ENST00000699700.1:n.1212C=
ENST00000699701.1:c.*145C=	ENSP00000514528.1:n.*145C=
ENST00000267415.12:c.765C= MANE Select	ENSP00000267415.7:p.Gly255=
ENST00000557921.2:c.657C=	ENSP00000453157.2:p.Gly219=
ENST00000646753.1:c.660C=	ENSP00000494065.1:p.Gly220=
ENST00000267415.11:c.765C=	ENSP00000267415.7:p.Gly255=
ENST00000399423.8:c.765C=	ENSP00000382350.4:p.Gly255=
ENST00000558476.5:c.327C=	ENSP00000452724.1:p.Gly109=
ENST00000558566.1:c.*137C=	ENSP00000453025.1:n.*137C=
ENST00000559019.1:c.*137C=	ENSP00000453675.1:n.*137C=
ENST00000559549.1:n.491C=
ENST00000559969.5:c.721C=
ENST00000626689.2:c.*137C=	ENSP00000486681.1:n.*137C=
NM_001099274.1:c.765C=	NP_001092744.1:p.Gly255=
NM_012461.2:c.765C=	NP_036593.2:p.Gly255=
XM_005267528.2:c.765C=	XP_005267585.1:p.Gly255=
XM_005267529.2:c.660C=	XP_005267586.1:p.Gly220=
NM_001099274.2:c.765C=	NP_001092744.1:p.Gly255=
NM_001363668.1:c.660C=	NP_001350597.1:p.Gly220=
NM_012461.3:c.765C=	NP_036593.2:p.Gly255=
XM_011536642.2:c.*145C=	XP_011534944.1:n.*145C=
XM_017021216.2:c.123C=	XP_016876705.1:p.Gly41=
XM_017021217.1:c.123C=	XP_016876706.1:p.Gly41=
NM_001099274.3:c.765C= MANE Select	NP_001092744.1:p.Gly255=
NM_001363668.2:c.660C=	NP_001350597.1:p.Gly220=