Canonical Allele Identifier: CA485782176

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24710014T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240808T>C , CM000676.2:g.24240808T>C	GRCh38
NC_000014.8:g.24710014T>C , CM000676.1:g.24710014T>C	GRCh37
NC_000014.7:g.23779854T>C	NCBI36
NG_016650.1:g.6867A>G
NG_054634.1:g.13392T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.975A>G
ENST00000557921.3:c.564A>G	ENSP00000453157.3:p.Arg188=
ENST00000699682.1:n.1062A>G
ENST00000699683.1:n.1112A>G
ENST00000699684.1:c.*265A>G	ENSP00000514523.1:n.*265A>G
ENST00000699685.1:n.876A>G
ENST00000699686.1:c.465A>G	ENSP00000514524.1:p.Arg155=
ENST00000699687.1:c.567A>G	ENSP00000514525.1:p.Arg189=
ENST00000699688.1:n.872A>G
ENST00000699689.1:n.1228A>G
ENST00000699690.1:n.1425A>G
ENST00000699691.1:n.1569A>G
ENST00000699693.1:n.1089A>G
ENST00000699694.1:n.1331A>G
ENST00000699695.1:c.*44A>G	ENSP00000514526.1:n.*44A>G
ENST00000699696.1:n.975A>G
ENST00000699697.1:c.672A>G	ENSP00000514527.1:p.Arg224=
ENST00000699698.1:n.593A>G
ENST00000699699.1:n.996A>G
ENST00000699700.1:n.1119A>G
ENST00000699701.1:c.*52A>G	ENSP00000514528.1:n.*52A>G
ENST00000267415.12:c.672A>G MANE Select	ENSP00000267415.7:p.Arg224=
ENST00000557921.2:c.564A>G	ENSP00000453157.2:p.Arg188=
ENST00000646753.1:c.567A>G	ENSP00000494065.1:p.Arg189=
ENST00000267415.11:c.672A>G	ENSP00000267415.7:p.Arg224=
ENST00000399423.8:c.672A>G	ENSP00000382350.4:p.Arg224=
ENST00000558476.5:c.234A>G	ENSP00000452724.1:p.Arg78=
ENST00000558566.1:c.*44A>G	ENSP00000453025.1:n.*44A>G
ENST00000559019.1:c.*44A>G	ENSP00000453675.1:n.*44A>G
ENST00000559549.1:n.398A>G
ENST00000559969.5:c.628A>G
ENST00000626689.2:c.*44A>G	ENSP00000486681.1:n.*44A>G
NM_001099274.1:c.672A>G	NP_001092744.1:p.Arg224=
NM_012461.2:c.672A>G	NP_036593.2:p.Arg224=
XM_005267528.2:c.672A>G	XP_005267585.1:p.Arg224=
XM_005267529.2:c.567A>G	XP_005267586.1:p.Arg189=
XM_011536642.1:c.*52A>G	XP_011534944.1:n.*52A>G
NM_001099274.2:c.672A>G	NP_001092744.1:p.Arg224=
NM_001363668.1:c.567A>G	NP_001350597.1:p.Arg189=
NM_012461.3:c.672A>G	NP_036593.2:p.Arg224=
XM_011536642.2:c.*52A>G	XP_011534944.1:n.*52A>G
XM_017021216.2:c.30A>G	XP_016876705.1:p.Arg10=
XM_017021217.1:c.30A>G	XP_016876706.1:p.Arg10=
NM_001099274.3:c.672A>G MANE Select	NP_001092744.1:p.Arg224=
NM_001363668.2:c.567A>G	NP_001350597.1:p.Arg189=