Canonical Allele Identifier: CA2123849321
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240668T= , CM000676.2:g.24240668T= GRCh38
NC_000014.8:g.24709874T= , CM000676.1:g.24709874T= GRCh37
NC_000014.7:g.23779714T= NCBI36
NG_016650.1:g.7007A=
NG_054634.1:g.13252T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1115A=
ENST00000557921.3:c.704A= ENSP00000453157.3:p.Gln235=
ENST00000699682.1:n.1202A=
ENST00000699683.1:n.1252A=
ENST00000699684.1:c.*405A= ENSP00000514523.1:n.*405A=
ENST00000699685.1:n.1016A=
ENST00000699686.1:c.605A= ENSP00000514524.1:p.Gln202=
ENST00000699687.1:c.707A= ENSP00000514525.1:p.Gln236=
ENST00000699688.1:n.1012A=
ENST00000699689.1:n.1368A=
ENST00000699690.1:n.1565A=
ENST00000699691.1:n.1709A=
ENST00000699693.1:n.1229A=
ENST00000699694.1:n.1471A=
ENST00000699695.1:c.*184A= ENSP00000514526.1:n.*184A=
ENST00000699696.1:n.1115A=
ENST00000699697.1:c.812A= ENSP00000514527.1:p.Gln271=
ENST00000699698.1:n.733A=
ENST00000699699.1:n.1136A=
ENST00000699700.1:n.1259A=
ENST00000699701.1:c.*192A= ENSP00000514528.1:n.*192A=
ENST00000267415.12:c.812A= MANE Select ENSP00000267415.7:p.Gln271=
ENST00000557921.2:c.704A= ENSP00000453157.2:p.Gln235=
ENST00000646753.1:c.707A= ENSP00000494065.1:p.Gln236=
ENST00000267415.11:c.812A= ENSP00000267415.7:p.Gln271=
ENST00000399423.8:c.812A= ENSP00000382350.4:p.Gln271=
ENST00000558476.5:c.374A= ENSP00000452724.1:p.Gln125=
ENST00000558566.1:c.*184A= ENSP00000453025.1:n.*184A=
ENST00000559019.1:c.*184A= ENSP00000453675.1:n.*184A=
ENST00000559549.1:n.538A=
ENST00000559969.5:c.757+11A=
ENST00000626689.2:c.*184A= ENSP00000486681.1:n.*184A=
NM_001099274.1:c.812A= NP_001092744.1:p.Gln271=
NM_012461.2:c.812A= NP_036593.2:p.Gln271=
XM_005267528.2:c.812A= XP_005267585.1:p.Gln271=
XM_005267529.2:c.707A= XP_005267586.1:p.Gln236=
NM_001099274.2:c.812A= NP_001092744.1:p.Gln271=
NM_001363668.1:c.707A= NP_001350597.1:p.Gln236=
NM_012461.3:c.812A= NP_036593.2:p.Gln271=
XM_011536642.2:c.*192A= XP_011534944.1:n.*192A=
XM_017021216.2:c.170A= XP_016876705.1:p.Gln57=
XM_017021217.1:c.170A= XP_016876706.1:p.Gln57=
NM_001099274.3:c.812A= MANE Select NP_001092744.1:p.Gln271=
NM_001363668.2:c.707A= NP_001350597.1:p.Gln236=