Canonical Allele Identifier: CA2695213971
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240655_24240656insT , CM000676.2:g.24240655_24240656insT GRCh38
NC_000014.8:g.24709861_24709862insT , CM000676.1:g.24709861_24709862insT GRCh37
NC_000014.7:g.23779701_23779702insT NCBI36
NG_016650.1:g.7019_7020insA
NG_054634.1:g.13239_13240insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000557915.2:n.1127_1128insA
ENST00000557921.3:c.716_717insA ENSP00000453157.3:p.Arg240Ter
ENST00000699682.1:n.1214_1215insA
ENST00000699683.1:n.1264_1265insA
ENST00000699684.1:c.*417_*418insA ENSP00000514523.1:n.*417_*418insA
ENST00000699685.1:n.1028_1029insA
ENST00000699686.1:c.617_618insA ENSP00000514524.1:p.Arg207Ter
ENST00000699687.1:c.719_720insA ENSP00000514525.1:p.Arg241Ter
ENST00000699688.1:n.1024_1025insA
ENST00000699689.1:n.1380_1381insA
ENST00000699690.1:n.1577_1578insA
ENST00000699691.1:n.1721_1722insA
ENST00000699693.1:n.1241_1242insA
ENST00000699694.1:n.1483_1484insA
ENST00000699695.1:c.*196_*197insA ENSP00000514526.1:n.*196_*197insA
ENST00000699696.1:n.1127_1128insA
ENST00000699697.1:c.824_825insA ENSP00000514527.1:p.Arg276Ter
ENST00000699698.1:n.745_746insA
ENST00000699699.1:n.1148_1149insA
ENST00000699700.1:n.1271_1272insA
ENST00000699701.1:c.*204_*205insA ENSP00000514528.1:n.*204_*205insA
ENST00000267415.12:c.824_825insA MANE Select ENSP00000267415.7:p.Arg276Ter
ENST00000557921.2:c.716_717insA ENSP00000453157.2:p.Arg240Ter
ENST00000646753.1:c.719_720insA ENSP00000494065.1:p.Arg241Ter
ENST00000267415.11:c.824_825insA ENSP00000267415.7:p.Arg276Ter
ENST00000399423.8:c.824_825insA ENSP00000382350.4:p.Arg276Ter
ENST00000558476.5:c.386_387insA ENSP00000452724.1:p.Arg130Ter
ENST00000558566.1:c.*196_*197insA ENSP00000453025.1:n.*196_*197insA
ENST00000559019.1:c.*196_*197insA ENSP00000453675.1:n.*196_*197insA
ENST00000559549.1:n.550_551insA
ENST00000559969.5:c.757+23_757+24insA
ENST00000626689.2:c.*196_*197insA ENSP00000486681.1:n.*196_*197insA
NM_001099274.1:c.824_825insA NP_001092744.1:p.Arg276Ter
NM_012461.2:c.824_825insA NP_036593.2:p.Arg276Ter
XM_005267528.2:c.824_825insA XP_005267585.1:p.Arg276Ter
XM_005267529.2:c.719_720insA XP_005267586.1:p.Arg241Ter
NM_001099274.2:c.824_825insA NP_001092744.1:p.Arg276Ter
NM_001363668.1:c.719_720insA NP_001350597.1:p.Arg241Ter
NM_012461.3:c.824_825insA NP_036593.2:p.Arg276Ter
XM_011536642.2:c.*204_*205insA XP_011534944.1:n.*204_*205insA
XM_017021216.2:c.182_183insA XP_016876705.1:p.Arg62Ter
XM_017021217.1:c.182_183insA XP_016876706.1:p.Arg62Ter
NM_001099274.3:c.824_825insA MANE Select NP_001092744.1:p.Arg276Ter
NM_001363668.2:c.719_720insA NP_001350597.1:p.Arg241Ter