Canonical Allele Identifier: CA2533693988
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240486_24240487insGA , CM000676.2:g.24240486_24240487insGA GRCh38
NC_000014.8:g.24709692_24709693insGA , CM000676.1:g.24709692_24709693insGA GRCh37
NC_000014.7:g.23779532_23779533insGA NCBI36
NG_016650.1:g.7189_7190insCT
NG_054634.1:g.13070_13071insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1297_1298insCT
ENST00000557921.3:c.886_887insCT ENSP00000453157.3:p.Cys296SerfsTer10
ENST00000699682.1:n.1384_1385insCT
ENST00000699683.1:n.1434_1435insCT
ENST00000699684.1:c.*587_*588insCT ENSP00000514523.1:n.*587_*588insCT
ENST00000699685.1:n.1198_1199insCT
ENST00000699686.1:c.787_788insCT ENSP00000514524.1:p.Cys263SerfsTer10
ENST00000699687.1:c.889_890insCT ENSP00000514525.1:p.Cys297SerfsTer10
ENST00000699688.1:n.1194_1195insCT
ENST00000699689.1:n.1550_1551insCT
ENST00000699690.1:n.1747_1748insCT
ENST00000699691.1:n.1891_1892insCT
ENST00000699693.1:n.1411_1412insCT
ENST00000699694.1:n.1653_1654insCT
ENST00000699695.1:c.*366_*367insCT ENSP00000514526.1:n.*366_*367insCT
ENST00000699696.1:n.1297_1298insCT
ENST00000699697.1:c.994_995insCT ENSP00000514527.1:p.Cys332SerfsTer10
ENST00000699698.1:n.915_916insCT
ENST00000699699.1:n.1318_1319insCT
ENST00000699700.1:n.1441_1442insCT
ENST00000699701.1:c.*374_*375insCT ENSP00000514528.1:n.*374_*375insCT
ENST00000267415.12:c.994_995insCT MANE Select ENSP00000267415.7:p.Cys332SerfsTer10
ENST00000646753.1:c.889_890insCT ENSP00000494065.1:p.Cys297SerfsTer10
ENST00000267415.11:c.994_995insCT ENSP00000267415.7:p.Cys332SerfsTer10
ENST00000399423.8:c.994_995insCT ENSP00000382350.4:p.Cys332SerfsTer10
ENST00000557915.1:n.113_114insCT
ENST00000558566.1:c.*366_*367insCT ENSP00000453025.1:n.*366_*367insCT
ENST00000559019.1:c.*366_*367insCT ENSP00000453675.1:n.*366_*367insCT
ENST00000559969.5:c.758-6_758-5insCT
ENST00000626689.2:c.*366_*367insCT ENSP00000486681.1:n.*366_*367insCT
NM_001099274.1:c.994_995insCT NP_001092744.1:p.Cys332SerfsTer10
NM_012461.2:c.994_995insCT NP_036593.2:p.Cys332SerfsTer10
XM_005267528.2:c.994_995insCT XP_005267585.1:p.Cys332SerfsTer10
XM_005267529.2:c.889_890insCT XP_005267586.1:p.Cys297SerfsTer10
NM_001099274.2:c.994_995insCT NP_001092744.1:p.Cys332SerfsTer10
NM_001363668.1:c.889_890insCT NP_001350597.1:p.Cys297SerfsTer10
NM_012461.3:c.994_995insCT NP_036593.2:p.Cys332SerfsTer10
XM_011536642.2:c.*374_*375insCT XP_011534944.1:n.*374_*375insCT
XM_017021216.2:c.352_353insCT XP_016876705.1:p.Cys118SerfsTer10
XM_017021217.1:c.352_353insCT XP_016876706.1:p.Cys118SerfsTer10
NM_001099274.3:c.994_995insCT MANE Select NP_001092744.1:p.Cys332SerfsTer10
NM_001363668.2:c.889_890insCT NP_001350597.1:p.Cys297SerfsTer10