Canonical Allele Identifier: CA485782106

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709484T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240278T>G , CM000676.2:g.24240278T>G	GRCh38
NC_000014.8:g.24709484T>G , CM000676.1:g.24709484T>G	GRCh37
NC_000014.7:g.23779324T>G	NCBI36
NG_016650.1:g.7397A>C
NG_054634.1:g.12862T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1505A>C
ENST00000557921.3:c.*137A>C	ENSP00000453157.3:n.*137A>C
ENST00000699682.1:n.1592A>C
ENST00000699683.1:n.1642A>C
ENST00000699684.1:c.*795A>C	ENSP00000514523.1:n.*795A>C
ENST00000699685.1:n.1406A>C
ENST00000699686.1:c.*137A>C	ENSP00000514524.1:n.*137A>C
ENST00000699687.1:c.*137A>C	ENSP00000514525.1:n.*137A>C
ENST00000699688.1:n.1402A>C
ENST00000699689.1:n.1758A>C
ENST00000699690.1:n.1955A>C
ENST00000699691.1:n.2099A>C
ENST00000699692.1:n.53A>C
ENST00000699693.1:n.1531A>C
ENST00000699694.1:n.1861A>C
ENST00000699695.1:c.*486A>C	ENSP00000514526.1:n.*486A>C
ENST00000699696.1:n.1505A>C
ENST00000699697.1:c.1114A>C	ENSP00000514527.1:p.Arg372=
ENST00000699698.1:n.1035A>C
ENST00000699699.1:n.1526A>C
ENST00000699700.1:n.1649A>C
ENST00000699701.1:c.*582A>C	ENSP00000514528.1:n.*582A>C
ENST00000267415.12:c.1114A>C MANE Select	ENSP00000267415.7:p.Arg372=
ENST00000646753.1:c.1009A>C	ENSP00000494065.1:p.Arg337=
ENST00000267415.11:c.1114A>C	ENSP00000267415.7:p.Arg372=
ENST00000399423.8:c.*137A>C	ENSP00000382350.4:n.*137A>C
ENST00000557915.1:n.321A>C
ENST00000558566.1:c.*574A>C	ENSP00000453025.1:n.*574A>C
ENST00000559969.5:c.960A>C
ENST00000560019.5:c.109A>C	ENSP00000453113.1:p.Arg37=
ENST00000626689.2:c.*486A>C	ENSP00000486681.1:n.*486A>C
NM_001099274.1:c.1114A>C	NP_001092744.1:p.Arg372=
NM_012461.2:c.*137A>C	NP_036593.2:n.*137A>C
XM_005267528.2:c.1114A>C	XP_005267585.1:p.Arg372=
XM_005267529.2:c.1009A>C	XP_005267586.1:p.Arg337=
NM_001099274.2:c.1114A>C	NP_001092744.1:p.Arg372=
NM_001363668.1:c.1009A>C	NP_001350597.1:p.Arg337=
NM_012461.3:c.*137A>C	NP_036593.2:n.*137A>C
XM_011536642.2:c.*582A>C	XP_011534944.1:n.*582A>C
XM_017021216.2:c.472A>C	XP_016876705.1:p.Arg158=
XM_017021217.1:c.472A>C	XP_016876706.1:p.Arg158=
NM_001099274.3:c.1114A>C MANE Select	NP_001092744.1:p.Arg372=
NM_001363668.2:c.1009A>C	NP_001350597.1:p.Arg337=