Canonical Allele Identifier: CA2123848820

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240284G= , CM000676.2:g.24240284G=	GRCh38
NC_000014.8:g.24709490G= , CM000676.1:g.24709490G=	GRCh37
NC_000014.7:g.23779330G=	NCBI36
NG_016650.1:g.7391C=
NG_054634.1:g.12868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1499C=
ENST00000557921.3:c.*131C=	ENSP00000453157.3:n.*131C=
ENST00000699682.1:n.1586C=
ENST00000699683.1:n.1636C=
ENST00000699684.1:c.*789C=	ENSP00000514523.1:n.*789C=
ENST00000699685.1:n.1400C=
ENST00000699686.1:c.*131C=	ENSP00000514524.1:n.*131C=
ENST00000699687.1:c.*131C=	ENSP00000514525.1:n.*131C=
ENST00000699688.1:n.1396C=
ENST00000699689.1:n.1752C=
ENST00000699690.1:n.1949C=
ENST00000699691.1:n.2093C=
ENST00000699692.1:n.47C=
ENST00000699693.1:n.1525C=
ENST00000699694.1:n.1855C=
ENST00000699695.1:c.*480C=	ENSP00000514526.1:n.*480C=
ENST00000699696.1:n.1499C=
ENST00000699697.1:c.1108C=	ENSP00000514527.1:p.Pro370=
ENST00000699698.1:n.1029C=
ENST00000699699.1:n.1520C=
ENST00000699700.1:n.1643C=
ENST00000699701.1:c.*576C=	ENSP00000514528.1:n.*576C=
ENST00000267415.12:c.1108C= MANE Select	ENSP00000267415.7:p.Pro370=
ENST00000646753.1:c.1003C=	ENSP00000494065.1:p.Pro335=
ENST00000267415.11:c.1108C=	ENSP00000267415.7:p.Pro370=
ENST00000399423.8:c.*131C=	ENSP00000382350.4:n.*131C=
ENST00000557915.1:n.315C=
ENST00000558566.1:c.*568C=	ENSP00000453025.1:n.*568C=
ENST00000559969.5:c.954C=
ENST00000560019.5:c.103C=	ENSP00000453113.1:p.Pro35=
ENST00000626689.2:c.*480C=	ENSP00000486681.1:n.*480C=
NM_001099274.1:c.1108C=	NP_001092744.1:p.Pro370=
NM_012461.2:c.*131C=	NP_036593.2:n.*131C=
XM_005267528.2:c.1108C=	XP_005267585.1:p.Pro370=
XM_005267529.2:c.1003C=	XP_005267586.1:p.Pro335=
NM_001099274.2:c.1108C=	NP_001092744.1:p.Pro370=
NM_001363668.1:c.1003C=	NP_001350597.1:p.Pro335=
NM_012461.3:c.*131C=	NP_036593.2:n.*131C=
XM_011536642.2:c.*576C=	XP_011534944.1:n.*576C=
XM_017021216.2:c.466C=	XP_016876705.1:p.Pro156=
XM_017021217.1:c.466C=	XP_016876706.1:p.Pro156=
NM_001099274.3:c.1108C= MANE Select	NP_001092744.1:p.Pro370=
NM_001363668.2:c.1003C=	NP_001350597.1:p.Pro335=