Canonical Allele Identifier: CA2123848938
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240313T= , CM000676.2:g.24240313T= GRCh38
NC_000014.8:g.24709519T= , CM000676.1:g.24709519T= GRCh37
NC_000014.7:g.23779359T= NCBI36
NG_016650.1:g.7362A=
NG_054634.1:g.12897T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1470A=
ENST00000557921.3:c.*102A= ENSP00000453157.3:n.*102A=
ENST00000699682.1:n.1557A=
ENST00000699683.1:n.1607A=
ENST00000699684.1:c.*760A= ENSP00000514523.1:n.*760A=
ENST00000699685.1:n.1371A=
ENST00000699686.1:c.*102A= ENSP00000514524.1:n.*102A=
ENST00000699687.1:c.*102A= ENSP00000514525.1:n.*102A=
ENST00000699688.1:n.1367A=
ENST00000699689.1:n.1723A=
ENST00000699690.1:n.1920A=
ENST00000699691.1:n.2064A=
ENST00000699692.1:n.18A=
ENST00000699693.1:n.1496A=
ENST00000699694.1:n.1826A=
ENST00000699695.1:c.*451A= ENSP00000514526.1:n.*451A=
ENST00000699696.1:n.1470A=
ENST00000699697.1:c.1079A= ENSP00000514527.1:p.Tyr360=
ENST00000699698.1:n.1000A=
ENST00000699699.1:n.1491A=
ENST00000699700.1:n.1614A=
ENST00000699701.1:c.*547A= ENSP00000514528.1:n.*547A=
ENST00000267415.12:c.1079A= MANE Select ENSP00000267415.7:p.Tyr360=
ENST00000646753.1:c.974A= ENSP00000494065.1:p.Tyr325=
ENST00000267415.11:c.1079A= ENSP00000267415.7:p.Tyr360=
ENST00000399423.8:c.*102A= ENSP00000382350.4:n.*102A=
ENST00000557915.1:n.286A=
ENST00000558566.1:c.*539A= ENSP00000453025.1:n.*539A=
ENST00000559969.5:c.925A=
ENST00000560019.5:c.74A= ENSP00000453113.1:p.Tyr25=
ENST00000626689.2:c.*451A= ENSP00000486681.1:n.*451A=
NM_001099274.1:c.1079A= NP_001092744.1:p.Tyr360=
NM_012461.2:c.*102A= NP_036593.2:n.*102A=
XM_005267528.2:c.1079A= XP_005267585.1:p.Tyr360=
XM_005267529.2:c.974A= XP_005267586.1:p.Tyr325=
NM_001099274.2:c.1079A= NP_001092744.1:p.Tyr360=
NM_001363668.1:c.974A= NP_001350597.1:p.Tyr325=
NM_012461.3:c.*102A= NP_036593.2:n.*102A=
XM_011536642.2:c.*547A= XP_011534944.1:n.*547A=
XM_017021216.2:c.437A= XP_016876705.1:p.Tyr146=
XM_017021217.1:c.437A= XP_016876706.1:p.Tyr146=
NM_001099274.3:c.1079A= MANE Select NP_001092744.1:p.Tyr360=
NM_001363668.2:c.974A= NP_001350597.1:p.Tyr325=