Canonical Allele Identifier: CA389226714
Gene: TINF2 HGNC NCBI

Linked Data

dbSNP Id: rs1308541264

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240732G>A , CM000676.2:g.24240732G>A GRCh38
NC_000014.8:g.24709938G>A , CM000676.1:g.24709938G>A GRCh37
NC_000014.7:g.23779778G>A NCBI36
NG_016650.1:g.6943C>T
NG_054634.1:g.13316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1051C>T
ENST00000557921.3:c.640C>T ENSP00000453157.3:p.Pro214Ser
ENST00000699682.1:n.1138C>T
ENST00000699683.1:n.1188C>T
ENST00000699684.1:c.*341C>T ENSP00000514523.1:n.*341C>T
ENST00000699685.1:n.952C>T
ENST00000699686.1:c.541C>T ENSP00000514524.1:p.Pro181Ser
ENST00000699687.1:c.643C>T ENSP00000514525.1:p.Pro215Ser
ENST00000699688.1:n.948C>T
ENST00000699689.1:n.1304C>T
ENST00000699690.1:n.1501C>T
ENST00000699691.1:n.1645C>T
ENST00000699693.1:n.1165C>T
ENST00000699694.1:n.1407C>T
ENST00000699695.1:c.*120C>T ENSP00000514526.1:n.*120C>T
ENST00000699696.1:n.1051C>T
ENST00000699697.1:c.748C>T ENSP00000514527.1:p.Pro250Ser
ENST00000699698.1:n.669C>T
ENST00000699699.1:n.1072C>T
ENST00000699700.1:n.1195C>T
ENST00000699701.1:c.*128C>T ENSP00000514528.1:n.*128C>T
ENST00000267415.12:c.748C>T MANE Select ENSP00000267415.7:p.Pro250Ser
ENST00000557921.2:c.640C>T ENSP00000453157.2:p.Pro214Ser
ENST00000646753.1:c.643C>T ENSP00000494065.1:p.Pro215Ser
ENST00000267415.11:c.748C>T ENSP00000267415.7:p.Pro250Ser
ENST00000399423.8:c.748C>T ENSP00000382350.4:p.Pro250Ser
ENST00000558476.5:c.310C>T ENSP00000452724.1:p.Pro104Ser
ENST00000558566.1:c.*120C>T ENSP00000453025.1:n.*120C>T
ENST00000559019.1:c.*120C>T ENSP00000453675.1:n.*120C>T
ENST00000559549.1:n.474C>T
ENST00000559969.5:c.704C>T
ENST00000626689.2:c.*120C>T ENSP00000486681.1:n.*120C>T
NM_001099274.1:c.748C>T NP_001092744.1:p.Pro250Ser
NM_012461.2:c.748C>T NP_036593.2:p.Pro250Ser
XM_005267528.2:c.748C>T XP_005267585.1:p.Pro250Ser
XM_005267529.2:c.643C>T XP_005267586.1:p.Pro215Ser
NM_001099274.2:c.748C>T NP_001092744.1:p.Pro250Ser
NM_001363668.1:c.643C>T NP_001350597.1:p.Pro215Ser
NM_012461.3:c.748C>T NP_036593.2:p.Pro250Ser
XM_011536642.2:c.*128C>T XP_011534944.1:n.*128C>T
XM_017021216.2:c.106C>T XP_016876705.1:p.Pro36Ser
XM_017021217.1:c.106C>T XP_016876706.1:p.Pro36Ser
NM_001099274.3:c.748C>T MANE Select NP_001092744.1:p.Pro250Ser
NM_001363668.2:c.643C>T NP_001350597.1:p.Pro215Ser