Canonical Allele Identifier: CA485782351
Gene: TINF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24709726T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240520T>C , CM000676.2:g.24240520T>C GRCh38
NC_000014.8:g.24709726T>C , CM000676.1:g.24709726T>C GRCh37
NC_000014.7:g.23779566T>C NCBI36
NG_016650.1:g.7155A>G
NG_054634.1:g.13104T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557915.2:n.1263A>G
ENST00000557921.3:c.852A>G ENSP00000453157.3:p.Thr284=
ENST00000699682.1:n.1350A>G
ENST00000699683.1:n.1400A>G
ENST00000699684.1:c.*553A>G ENSP00000514523.1:n.*553A>G
ENST00000699685.1:n.1164A>G
ENST00000699686.1:c.753A>G ENSP00000514524.1:p.Thr251=
ENST00000699687.1:c.855A>G ENSP00000514525.1:p.Thr285=
ENST00000699688.1:n.1160A>G
ENST00000699689.1:n.1516A>G
ENST00000699690.1:n.1713A>G
ENST00000699691.1:n.1857A>G
ENST00000699693.1:n.1377A>G
ENST00000699694.1:n.1619A>G
ENST00000699695.1:c.*332A>G ENSP00000514526.1:n.*332A>G
ENST00000699696.1:n.1263A>G
ENST00000699697.1:c.960A>G ENSP00000514527.1:p.Thr320=
ENST00000699698.1:n.881A>G
ENST00000699699.1:n.1284A>G
ENST00000699700.1:n.1407A>G
ENST00000699701.1:c.*340A>G ENSP00000514528.1:n.*340A>G
ENST00000267415.12:c.960A>G MANE Select ENSP00000267415.7:p.Thr320=
ENST00000557921.2:c.852A>G ENSP00000453157.2:p.Thr284=
ENST00000646753.1:c.855A>G ENSP00000494065.1:p.Thr285=
ENST00000267415.11:c.960A>G ENSP00000267415.7:p.Thr320=
ENST00000399423.8:c.960A>G ENSP00000382350.4:p.Thr320=
ENST00000557915.1:n.79A>G
ENST00000558566.1:c.*332A>G ENSP00000453025.1:n.*332A>G
ENST00000559019.1:c.*332A>G ENSP00000453675.1:n.*332A>G
ENST00000559969.5:c.758-40A>G
ENST00000626689.2:c.*332A>G ENSP00000486681.1:n.*332A>G
NM_001099274.1:c.960A>G NP_001092744.1:p.Thr320=
NM_012461.2:c.960A>G NP_036593.2:p.Thr320=
XM_005267528.2:c.960A>G XP_005267585.1:p.Thr320=
XM_005267529.2:c.855A>G XP_005267586.1:p.Thr285=
NM_001099274.2:c.960A>G NP_001092744.1:p.Thr320=
NM_001363668.1:c.855A>G NP_001350597.1:p.Thr285=
NM_012461.3:c.960A>G NP_036593.2:p.Thr320=
XM_011536642.2:c.*340A>G XP_011534944.1:n.*340A>G
XM_017021216.2:c.318A>G XP_016876705.1:p.Thr106=
XM_017021217.1:c.318A>G XP_016876706.1:p.Thr106=
NM_001099274.3:c.960A>G MANE Select NP_001092744.1:p.Thr320=
NM_001363668.2:c.855A>G NP_001350597.1:p.Thr285=