Canonical Allele Identifier: CA2123848965
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240318A= , CM000676.2:g.24240318A= GRCh38
NC_000014.8:g.24709524A= , CM000676.1:g.24709524A= GRCh37
NC_000014.7:g.23779364A= NCBI36
NG_016650.1:g.7357T=
NG_054634.1:g.12902A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1465T=
ENST00000557921.3:c.*97T= ENSP00000453157.3:n.*97T=
ENST00000699682.1:n.1552T=
ENST00000699683.1:n.1602T=
ENST00000699684.1:c.*755T= ENSP00000514523.1:n.*755T=
ENST00000699685.1:n.1366T=
ENST00000699686.1:c.*97T= ENSP00000514524.1:n.*97T=
ENST00000699687.1:c.*97T= ENSP00000514525.1:n.*97T=
ENST00000699688.1:n.1362T=
ENST00000699689.1:n.1718T=
ENST00000699690.1:n.1915T=
ENST00000699691.1:n.2059T=
ENST00000699692.1:n.13T=
ENST00000699693.1:n.1491T=
ENST00000699694.1:n.1821T=
ENST00000699695.1:c.*446T= ENSP00000514526.1:n.*446T=
ENST00000699696.1:n.1465T=
ENST00000699697.1:c.1074T= ENSP00000514527.1:p.Asp358=
ENST00000699698.1:n.995T=
ENST00000699699.1:n.1486T=
ENST00000699700.1:n.1609T=
ENST00000699701.1:c.*542T= ENSP00000514528.1:n.*542T=
ENST00000267415.12:c.1074T= MANE Select ENSP00000267415.7:p.Asp358=
ENST00000646753.1:c.969T= ENSP00000494065.1:p.Asp323=
ENST00000267415.11:c.1074T= ENSP00000267415.7:p.Asp358=
ENST00000399423.8:c.*97T= ENSP00000382350.4:n.*97T=
ENST00000557915.1:n.281T=
ENST00000558566.1:c.*534T= ENSP00000453025.1:n.*534T=
ENST00000559969.5:c.920T=
ENST00000560019.5:c.69T= ENSP00000453113.1:p.Asp23=
ENST00000626689.2:c.*446T= ENSP00000486681.1:n.*446T=
NM_001099274.1:c.1074T= NP_001092744.1:p.Asp358=
NM_012461.2:c.*97T= NP_036593.2:n.*97T=
XM_005267528.2:c.1074T= XP_005267585.1:p.Asp358=
XM_005267529.2:c.969T= XP_005267586.1:p.Asp323=
NM_001099274.2:c.1074T= NP_001092744.1:p.Asp358=
NM_001363668.1:c.969T= NP_001350597.1:p.Asp323=
NM_012461.3:c.*97T= NP_036593.2:n.*97T=
XM_011536642.2:c.*542T= XP_011534944.1:n.*542T=
XM_017021216.2:c.432T= XP_016876705.1:p.Asp144=
XM_017021217.1:c.432T= XP_016876706.1:p.Asp144=
NM_001099274.3:c.1074T= MANE Select NP_001092744.1:p.Asp358=
NM_001363668.2:c.969T= NP_001350597.1:p.Asp323=