Canonical Allele Identifier: CA2123849370
Community Standard Title: NM_001099274.3(TINF2):c.706C= (p.Pro236=)
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240774G= , CM000676.2:g.24240774G= GRCh38
NC_000014.8:g.24709980G= , CM000676.1:g.24709980G= GRCh37
NC_000014.7:g.23779820G= NCBI36
NG_016650.1:g.6901C=
NG_054634.1:g.13358G=

Transcript Alleles

HGVS Amino-acid Change
NM_001099274.3:c.706C= MANE Select NP_001092744.1:p.Pro236=
ENST00000267415.12:c.706C= MANE Select ENSP00000267415.7:p.Pro236=
NM_001099274.1:c.706C= NP_001092744.1:p.Pro236=
NM_001099274.2:c.706C= NP_001092744.1:p.Pro236=
NM_001363668.1:c.601C= NP_001350597.1:p.Pro201=
NM_001363668.2:c.601C= NP_001350597.1:p.Pro201=
NM_012461.2:c.706C= NP_036593.2:p.Pro236=
NM_012461.3:c.706C= NP_036593.2:p.Pro236=
ENST00000267415.11:c.706C= ENSP00000267415.7:p.Pro236=
ENST00000399423.8:c.706C= ENSP00000382350.4:p.Pro236=
ENST00000557915.2:n.1009C=
ENST00000557921.2:c.598C= ENSP00000453157.2:p.Pro200=
ENST00000557921.3:c.598C= ENSP00000453157.3:p.Pro200=
ENST00000558476.5:c.268C= ENSP00000452724.1:p.Pro90=
ENST00000558566.1:c.*78C= ENSP00000453025.1:n.*78C=
ENST00000559019.1:c.*78C= ENSP00000453675.1:n.*78C=
ENST00000559549.1:n.432C=
ENST00000559969.5:c.662C=
ENST00000626689.2:c.*78C= ENSP00000486681.1:n.*78C=
ENST00000646753.1:c.601C= ENSP00000494065.1:p.Pro201=
ENST00000699682.1:n.1096C=
ENST00000699683.1:n.1146C=
ENST00000699684.1:c.*299C= ENSP00000514523.1:n.*299C=
ENST00000699685.1:n.910C=
ENST00000699686.1:c.499C= ENSP00000514524.1:p.Pro167=
ENST00000699687.1:c.601C= ENSP00000514525.1:p.Pro201=
ENST00000699688.1:n.906C=
ENST00000699689.1:n.1262C=
ENST00000699690.1:n.1459C=
ENST00000699691.1:n.1603C=
ENST00000699693.1:n.1123C=
ENST00000699694.1:n.1365C=
ENST00000699695.1:c.*78C= ENSP00000514526.1:n.*78C=
ENST00000699696.1:n.1009C=
ENST00000699697.1:c.706C= ENSP00000514527.1:p.Pro236=
ENST00000699698.1:n.627C=
ENST00000699699.1:n.1030C=
ENST00000699700.1:n.1153C=
ENST00000699701.1:c.*86C= ENSP00000514528.1:n.*86C=
XM_005267528.2:c.706C= XP_005267585.1:p.Pro236=
XM_005267529.2:c.601C= XP_005267586.1:p.Pro201=
XM_011536642.2:c.*86C= XP_011534944.1:n.*86C=
XM_017021216.2:c.64C= XP_016876705.1:p.Pro22=
XM_017021217.1:c.64C= XP_016876706.1:p.Pro22=