Canonical Allele Identifier: CA2123849295

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240624T= , CM000676.2:g.24240624T=	GRCh38
NC_000014.8:g.24709830T= , CM000676.1:g.24709830T=	GRCh37
NC_000014.7:g.23779670T=	NCBI36
NG_016650.1:g.7051A=
NG_054634.1:g.13208T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1159A=
ENST00000557921.3:c.748A=	ENSP00000453157.3:p.Met250=
ENST00000699682.1:n.1246A=
ENST00000699683.1:n.1296A=
ENST00000699684.1:c.*449A=	ENSP00000514523.1:n.*449A=
ENST00000699685.1:n.1060A=
ENST00000699686.1:c.649A=	ENSP00000514524.1:p.Met217=
ENST00000699687.1:c.751A=	ENSP00000514525.1:p.Met251=
ENST00000699688.1:n.1056A=
ENST00000699689.1:n.1412A=
ENST00000699690.1:n.1609A=
ENST00000699691.1:n.1753A=
ENST00000699693.1:n.1273A=
ENST00000699694.1:n.1515A=
ENST00000699695.1:c.*228A=	ENSP00000514526.1:n.*228A=
ENST00000699696.1:n.1159A=
ENST00000699697.1:c.856A=	ENSP00000514527.1:p.Met286=
ENST00000699698.1:n.777A=
ENST00000699699.1:n.1180A=
ENST00000699700.1:n.1303A=
ENST00000699701.1:c.*236A=	ENSP00000514528.1:n.*236A=
ENST00000267415.12:c.856A= MANE Select	ENSP00000267415.7:p.Met286=
ENST00000557921.2:c.748A=	ENSP00000453157.2:p.Met250=
ENST00000646753.1:c.751A=	ENSP00000494065.1:p.Met251=
ENST00000267415.11:c.856A=	ENSP00000267415.7:p.Met286=
ENST00000399423.8:c.856A=	ENSP00000382350.4:p.Met286=
ENST00000558476.5:c.418A=	ENSP00000452724.1:p.Met140=
ENST00000558566.1:c.*228A=	ENSP00000453025.1:n.*228A=
ENST00000559019.1:c.*228A=	ENSP00000453675.1:n.*228A=
ENST00000559549.1:n.582A=
ENST00000559969.5:c.757+55A=
ENST00000626689.2:c.*228A=	ENSP00000486681.1:n.*228A=
NM_001099274.1:c.856A=	NP_001092744.1:p.Met286=
NM_012461.2:c.856A=	NP_036593.2:p.Met286=
XM_005267528.2:c.856A=	XP_005267585.1:p.Met286=
XM_005267529.2:c.751A=	XP_005267586.1:p.Met251=
NM_001099274.2:c.856A=	NP_001092744.1:p.Met286=
NM_001363668.1:c.751A=	NP_001350597.1:p.Met251=
NM_012461.3:c.856A=	NP_036593.2:p.Met286=
XM_011536642.2:c.*236A=	XP_011534944.1:n.*236A=
XM_017021216.2:c.214A=	XP_016876705.1:p.Met72=
XM_017021217.1:c.214A=	XP_016876706.1:p.Met72=
NM_001099274.3:c.856A= MANE Select	NP_001092744.1:p.Met286=
NM_001363668.2:c.751A=	NP_001350597.1:p.Met251=