Canonical Allele Identifier: CA2123849142
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240437G= , CM000676.2:g.24240437G= GRCh38
NC_000014.8:g.24709643G= , CM000676.1:g.24709643G= GRCh37
NC_000014.7:g.23779483G= NCBI36
NG_016650.1:g.7238C=
NG_054634.1:g.13021G=

Transcript Alleles

HGVS Amino-acid change
ENST00000557915.2:n.1346C=
ENST00000557921.3:c.935C= ENSP00000453157.3:p.Pro312=
ENST00000699682.1:n.1433C=
ENST00000699683.1:n.1483C=
ENST00000699684.1:c.*636C= ENSP00000514523.1:n.*636C=
ENST00000699685.1:n.1247C=
ENST00000699686.1:c.836C= ENSP00000514524.1:p.Pro279=
ENST00000699687.1:c.938C= ENSP00000514525.1:p.Pro313=
ENST00000699688.1:n.1243C=
ENST00000699689.1:n.1599C=
ENST00000699690.1:n.1796C=
ENST00000699691.1:n.1940C=
ENST00000699693.1:n.1460C=
ENST00000699694.1:n.1702C=
ENST00000699695.1:c.*415C= ENSP00000514526.1:n.*415C=
ENST00000699696.1:n.1346C=
ENST00000699697.1:c.1043C= ENSP00000514527.1:p.Pro348=
ENST00000699698.1:n.964C=
ENST00000699699.1:n.1367C=
ENST00000699700.1:n.1490C=
ENST00000699701.1:c.*423C= ENSP00000514528.1:n.*423C=
ENST00000267415.12:c.1043C= MANE Select ENSP00000267415.7:p.Pro348=
ENST00000646753.1:c.938C= ENSP00000494065.1:p.Pro313=
ENST00000267415.11:c.1043C= ENSP00000267415.7:p.Pro348=
ENST00000399423.8:c.1043C= ENSP00000382350.4:p.Pro348=
ENST00000557915.1:n.162C=
ENST00000558566.1:c.*415C= ENSP00000453025.1:n.*415C=
ENST00000559969.5:c.801C=
ENST00000560019.5:c.38C= ENSP00000453113.1:p.Pro13=
ENST00000626689.2:c.*415C= ENSP00000486681.1:n.*415C=
NM_001099274.1:c.1043C= NP_001092744.1:p.Pro348=
NM_012461.2:c.1043C= NP_036593.2:p.Pro348=
XM_005267528.2:c.1043C= XP_005267585.1:p.Pro348=
XM_005267529.2:c.938C= XP_005267586.1:p.Pro313=
NM_001099274.2:c.1043C= NP_001092744.1:p.Pro348=
NM_001363668.1:c.938C= NP_001350597.1:p.Pro313=
NM_012461.3:c.1043C= NP_036593.2:p.Pro348=
XM_011536642.2:c.*423C= XP_011534944.1:n.*423C=
XM_017021216.2:c.401C= XP_016876705.1:p.Pro134=
XM_017021217.1:c.401C= XP_016876706.1:p.Pro134=
NM_001099274.3:c.1043C= MANE Select NP_001092744.1:p.Pro348=
NM_001363668.2:c.938C= NP_001350597.1:p.Pro313=