Canonical Allele Identifier: CA2123849300

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240632G= , CM000676.2:g.24240632G=	GRCh38
NC_000014.8:g.24709838G= , CM000676.1:g.24709838G=	GRCh37
NC_000014.7:g.23779678G=	NCBI36
NG_016650.1:g.7043C=
NG_054634.1:g.13216G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1151C=
ENST00000557921.3:c.740C=	ENSP00000453157.3:p.Pro247=
ENST00000699682.1:n.1238C=
ENST00000699683.1:n.1288C=
ENST00000699684.1:c.*441C=	ENSP00000514523.1:n.*441C=
ENST00000699685.1:n.1052C=
ENST00000699686.1:c.641C=	ENSP00000514524.1:p.Pro214=
ENST00000699687.1:c.743C=	ENSP00000514525.1:p.Pro248=
ENST00000699688.1:n.1048C=
ENST00000699689.1:n.1404C=
ENST00000699690.1:n.1601C=
ENST00000699691.1:n.1745C=
ENST00000699693.1:n.1265C=
ENST00000699694.1:n.1507C=
ENST00000699695.1:c.*220C=	ENSP00000514526.1:n.*220C=
ENST00000699696.1:n.1151C=
ENST00000699697.1:c.848C=	ENSP00000514527.1:p.Pro283=
ENST00000699698.1:n.769C=
ENST00000699699.1:n.1172C=
ENST00000699700.1:n.1295C=
ENST00000699701.1:c.*228C=	ENSP00000514528.1:n.*228C=
ENST00000267415.12:c.848C= MANE Select	ENSP00000267415.7:p.Pro283=
ENST00000557921.2:c.740C=	ENSP00000453157.2:p.Pro247=
ENST00000646753.1:c.743C=	ENSP00000494065.1:p.Pro248=
ENST00000267415.11:c.848C=	ENSP00000267415.7:p.Pro283=
ENST00000399423.8:c.848C=	ENSP00000382350.4:p.Pro283=
ENST00000558476.5:c.410C=	ENSP00000452724.1:p.Pro137=
ENST00000558566.1:c.*220C=	ENSP00000453025.1:n.*220C=
ENST00000559019.1:c.*220C=	ENSP00000453675.1:n.*220C=
ENST00000559549.1:n.574C=
ENST00000559969.5:c.757+47C=
ENST00000626689.2:c.*220C=	ENSP00000486681.1:n.*220C=
NM_001099274.1:c.848C=	NP_001092744.1:p.Pro283=
NM_012461.2:c.848C=	NP_036593.2:p.Pro283=
XM_005267528.2:c.848C=	XP_005267585.1:p.Pro283=
XM_005267529.2:c.743C=	XP_005267586.1:p.Pro248=
NM_001099274.2:c.848C=	NP_001092744.1:p.Pro283=
NM_001363668.1:c.743C=	NP_001350597.1:p.Pro248=
NM_012461.3:c.848C=	NP_036593.2:p.Pro283=
XM_011536642.2:c.*228C=	XP_011534944.1:n.*228C=
XM_017021216.2:c.206C=	XP_016876705.1:p.Pro69=
XM_017021217.1:c.206C=	XP_016876706.1:p.Pro69=
NM_001099274.3:c.848C= MANE Select	NP_001092744.1:p.Pro283=
NM_001363668.2:c.743C=	NP_001350597.1:p.Pro248=