Canonical Allele Identifier: CA2123848975

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240327A= , CM000676.2:g.24240327A=	GRCh38
NC_000014.8:g.24709533A= , CM000676.1:g.24709533A=	GRCh37
NC_000014.7:g.23779373A=	NCBI36
NG_016650.1:g.7348T=
NG_054634.1:g.12911A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1456T=
ENST00000557921.3:c.*88T=	ENSP00000453157.3:n.*88T=
ENST00000699682.1:n.1543T=
ENST00000699683.1:n.1593T=
ENST00000699684.1:c.*746T=	ENSP00000514523.1:n.*746T=
ENST00000699685.1:n.1357T=
ENST00000699686.1:c.*88T=	ENSP00000514524.1:n.*88T=
ENST00000699687.1:c.*88T=	ENSP00000514525.1:n.*88T=
ENST00000699688.1:n.1353T=
ENST00000699689.1:n.1709T=
ENST00000699690.1:n.1906T=
ENST00000699691.1:n.2050T=
ENST00000699692.1:n.4T=
ENST00000699693.1:n.1482T=
ENST00000699694.1:n.1812T=
ENST00000699695.1:c.*437T=	ENSP00000514526.1:n.*437T=
ENST00000699696.1:n.1456T=
ENST00000699697.1:c.1065T=	ENSP00000514527.1:p.Asn355=
ENST00000699698.1:n.986T=
ENST00000699699.1:n.1477T=
ENST00000699700.1:n.1600T=
ENST00000699701.1:c.*533T=	ENSP00000514528.1:n.*533T=
ENST00000267415.12:c.1065T= MANE Select	ENSP00000267415.7:p.Asn355=
ENST00000646753.1:c.960T=	ENSP00000494065.1:p.Asn320=
ENST00000267415.11:c.1065T=	ENSP00000267415.7:p.Asn355=
ENST00000399423.8:c.*88T=	ENSP00000382350.4:n.*88T=
ENST00000557915.1:n.272T=
ENST00000558566.1:c.*525T=	ENSP00000453025.1:n.*525T=
ENST00000559969.5:c.911T=
ENST00000560019.5:c.60T=	ENSP00000453113.1:p.Asn20=
ENST00000626689.2:c.*437T=	ENSP00000486681.1:n.*437T=
NM_001099274.1:c.1065T=	NP_001092744.1:p.Asn355=
NM_012461.2:c.*88T=	NP_036593.2:n.*88T=
XM_005267528.2:c.1065T=	XP_005267585.1:p.Asn355=
XM_005267529.2:c.960T=	XP_005267586.1:p.Asn320=
NM_001099274.2:c.1065T=	NP_001092744.1:p.Asn355=
NM_001363668.1:c.960T=	NP_001350597.1:p.Asn320=
NM_012461.3:c.*88T=	NP_036593.2:n.*88T=
XM_011536642.2:c.*533T=	XP_011534944.1:n.*533T=
XM_017021216.2:c.423T=	XP_016876705.1:p.Asn141=
XM_017021217.1:c.423T=	XP_016876706.1:p.Asn141=
NM_001099274.3:c.1065T= MANE Select	NP_001092744.1:p.Asn355=
NM_001363668.2:c.960T=	NP_001350597.1:p.Asn320=