Canonical Allele Identifier: CA2123849026
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240354G= , CM000676.2:g.24240354G= GRCh38
NC_000014.8:g.24709560G= , CM000676.1:g.24709560G= GRCh37
NC_000014.7:g.23779400G= NCBI36
NG_016650.1:g.7321C=
NG_054634.1:g.12938G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1429C=
ENST00000557921.3:c.*61C= ENSP00000453157.3:n.*61C=
ENST00000699682.1:n.1516C=
ENST00000699683.1:n.1566C=
ENST00000699684.1:c.*719C= ENSP00000514523.1:n.*719C=
ENST00000699685.1:n.1330C=
ENST00000699686.1:c.*61C= ENSP00000514524.1:n.*61C=
ENST00000699687.1:c.*61C= ENSP00000514525.1:n.*61C=
ENST00000699688.1:n.1326C=
ENST00000699689.1:n.1682C=
ENST00000699690.1:n.1879C=
ENST00000699691.1:n.2023C=
ENST00000699693.1:n.1479-24C=
ENST00000699694.1:n.1785C=
ENST00000699695.1:c.*434-24C= ENSP00000514526.1:n.*434-24C=
ENST00000699696.1:n.1429C=
ENST00000699697.1:c.1062-24C= ENSP00000514527.1:n.1062-24C=
ENST00000699698.1:n.983-24C=
ENST00000699699.1:n.1450C=
ENST00000699700.1:n.1573C=
ENST00000699701.1:c.*506C= ENSP00000514528.1:n.*506C=
ENST00000267415.12:c.1062-24C= MANE Select ENSP00000267415.7:n.1062-24C=
ENST00000646753.1:c.957-24C= ENSP00000494065.1:n.957-24C=
ENST00000267415.11:c.1062-24C= ENSP00000267415.7:n.1062-24C=
ENST00000399423.8:c.*61C= ENSP00000382350.4:n.*61C=
ENST00000557915.1:n.245C=
ENST00000558566.1:c.*498C= ENSP00000453025.1:n.*498C=
ENST00000559969.5:c.884C=
ENST00000560019.5:c.57-24C= ENSP00000453113.1:n.57-24C=
ENST00000626689.2:c.*434-24C= ENSP00000486681.1:n.*434-24C=
NM_001099274.1:c.1062-24C= NP_001092744.1:n.1062-24C=
NM_012461.2:c.*61C= NP_036593.2:n.*61C=
XM_005267528.2:c.1062-24C= XP_005267585.1:n.1062-24C=
XM_005267529.2:c.957-24C= XP_005267586.1:n.957-24C=
NM_001099274.2:c.1062-24C= NP_001092744.1:n.1062-24C=
NM_001363668.1:c.957-24C= NP_001350597.1:n.957-24C=
NM_012461.3:c.*61C= NP_036593.2:n.*61C=
XM_011536642.2:c.*506C= XP_011534944.1:n.*506C=
XM_017021216.2:c.420-24C= XP_016876705.1:n.420-24C=
XM_017021217.1:c.420-24C= XP_016876706.1:n.420-24C=
NM_001099274.3:c.1062-24C= MANE Select NP_001092744.1:n.1062-24C=
NM_001363668.2:c.957-24C= NP_001350597.1:n.957-24C=