Canonical Allele Identifier: CA2123849290
Gene: TINF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24240614_24240615delinsGG , CM000676.2:g.24240614_24240615delinsGG GRCh38
NC_000014.8:g.24709820_24709821delinsGG , CM000676.1:g.24709820_24709821delinsGG GRCh37
NC_000014.7:g.23779660_23779661delinsGG NCBI36
NG_016650.1:g.7060_7061delinsCC
NG_054634.1:g.13198_13199delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000557915.2:n.1168_1169delinsCC
ENST00000557921.3:c.757_758delinsCC ENSP00000453157.3:p.Pro253=
ENST00000699682.1:n.1255_1256delinsCC
ENST00000699683.1:n.1305_1306delinsCC
ENST00000699684.1:c.*458_*459delinsCC ENSP00000514523.1:n.*458_*459delinsCC
ENST00000699685.1:n.1069_1070delinsCC
ENST00000699686.1:c.658_659delinsCC ENSP00000514524.1:p.Pro220=
ENST00000699687.1:c.760_761delinsCC ENSP00000514525.1:p.Pro254=
ENST00000699688.1:n.1065_1066delinsCC
ENST00000699689.1:n.1421_1422delinsCC
ENST00000699690.1:n.1618_1619delinsCC
ENST00000699691.1:n.1762_1763delinsCC
ENST00000699693.1:n.1282_1283delinsCC
ENST00000699694.1:n.1524_1525delinsCC
ENST00000699695.1:c.*237_*238delinsCC ENSP00000514526.1:n.*237_*238delinsCC
ENST00000699696.1:n.1168_1169delinsCC
ENST00000699697.1:c.865_866delinsCC ENSP00000514527.1:p.Pro289=
ENST00000699698.1:n.786_787delinsCC
ENST00000699699.1:n.1189_1190delinsCC
ENST00000699700.1:n.1312_1313delinsCC
ENST00000699701.1:c.*245_*246delinsCC ENSP00000514528.1:n.*245_*246delinsCC
ENST00000267415.12:c.865_866delinsCC MANE Select ENSP00000267415.7:p.Pro289=
ENST00000557921.2:c.757_758delinsCC ENSP00000453157.2:p.Pro253=
ENST00000646753.1:c.760_761delinsCC ENSP00000494065.1:p.Pro254=
ENST00000267415.11:c.865_866delinsCC ENSP00000267415.7:p.Pro289=
ENST00000399423.8:c.865_866delinsCC ENSP00000382350.4:p.Pro289=
ENST00000558476.5:c.427_428delinsCC ENSP00000452724.1:p.Pro143=
ENST00000558566.1:c.*237_*238delinsCC ENSP00000453025.1:n.*237_*238delinsCC
ENST00000559019.1:c.*237_*238delinsCC ENSP00000453675.1:n.*237_*238delinsCC
ENST00000559549.1:n.591_592delinsCC
ENST00000559969.5:c.757+64_757+65delinsCC
ENST00000626689.2:c.*237_*238delinsCC ENSP00000486681.1:n.*237_*238delinsCC
NM_001099274.1:c.865_866delinsCC NP_001092744.1:p.Pro289=
NM_012461.2:c.865_866delinsCC NP_036593.2:p.Pro289=
XM_005267528.2:c.865_866delinsCC XP_005267585.1:p.Pro289=
XM_005267529.2:c.760_761delinsCC XP_005267586.1:p.Pro254=
NM_001099274.2:c.865_866delinsCC NP_001092744.1:p.Pro289=
NM_001363668.1:c.760_761delinsCC NP_001350597.1:p.Pro254=
NM_012461.3:c.865_866delinsCC NP_036593.2:p.Pro289=
XM_011536642.2:c.*245_*246delinsCC XP_011534944.1:n.*245_*246delinsCC
XM_017021216.2:c.223_224delinsCC XP_016876705.1:p.Pro75=
XM_017021217.1:c.223_224delinsCC XP_016876706.1:p.Pro75=
NM_001099274.3:c.865_866delinsCC MANE Select NP_001092744.1:p.Pro289=
NM_001363668.2:c.760_761delinsCC NP_001350597.1:p.Pro254=