Canonical Allele Identifier: CA2123849339

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240703A= , CM000676.2:g.24240703A=	GRCh38
NC_000014.8:g.24709909A= , CM000676.1:g.24709909A=	GRCh37
NC_000014.7:g.23779749A=	NCBI36
NG_016650.1:g.6972T=
NG_054634.1:g.13287A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1080T=
ENST00000557921.3:c.669T=	ENSP00000453157.3:p.Asn223=
ENST00000699682.1:n.1167T=
ENST00000699683.1:n.1217T=
ENST00000699684.1:c.*370T=	ENSP00000514523.1:n.*370T=
ENST00000699685.1:n.981T=
ENST00000699686.1:c.570T=	ENSP00000514524.1:p.Asn190=
ENST00000699687.1:c.672T=	ENSP00000514525.1:p.Asn224=
ENST00000699688.1:n.977T=
ENST00000699689.1:n.1333T=
ENST00000699690.1:n.1530T=
ENST00000699691.1:n.1674T=
ENST00000699693.1:n.1194T=
ENST00000699694.1:n.1436T=
ENST00000699695.1:c.*149T=	ENSP00000514526.1:n.*149T=
ENST00000699696.1:n.1080T=
ENST00000699697.1:c.777T=	ENSP00000514527.1:p.Asn259=
ENST00000699698.1:n.698T=
ENST00000699699.1:n.1101T=
ENST00000699700.1:n.1224T=
ENST00000699701.1:c.*157T=	ENSP00000514528.1:n.*157T=
ENST00000267415.12:c.777T= MANE Select	ENSP00000267415.7:p.Asn259=
ENST00000557921.2:c.669T=	ENSP00000453157.2:p.Asn223=
ENST00000646753.1:c.672T=	ENSP00000494065.1:p.Asn224=
ENST00000267415.11:c.777T=	ENSP00000267415.7:p.Asn259=
ENST00000399423.8:c.777T=	ENSP00000382350.4:p.Asn259=
ENST00000558476.5:c.339T=	ENSP00000452724.1:p.Asn113=
ENST00000558566.1:c.*149T=	ENSP00000453025.1:n.*149T=
ENST00000559019.1:c.*149T=	ENSP00000453675.1:n.*149T=
ENST00000559549.1:n.503T=
ENST00000559969.5:c.733T=
ENST00000626689.2:c.*149T=	ENSP00000486681.1:n.*149T=
NM_001099274.1:c.777T=	NP_001092744.1:p.Asn259=
NM_012461.2:c.777T=	NP_036593.2:p.Asn259=
XM_005267528.2:c.777T=	XP_005267585.1:p.Asn259=
XM_005267529.2:c.672T=	XP_005267586.1:p.Asn224=
NM_001099274.2:c.777T=	NP_001092744.1:p.Asn259=
NM_001363668.1:c.672T=	NP_001350597.1:p.Asn224=
NM_012461.3:c.777T=	NP_036593.2:p.Asn259=
XM_011536642.2:c.*157T=	XP_011534944.1:n.*157T=
XM_017021216.2:c.135T=	XP_016876705.1:p.Asn45=
XM_017021217.1:c.135T=	XP_016876706.1:p.Asn45=
NM_001099274.3:c.777T= MANE Select	NP_001092744.1:p.Asn259=
NM_001363668.2:c.672T=	NP_001350597.1:p.Asn224=