Canonical Allele Identifier: CA2624345197

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240403-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240406_24240407del , CM000676.2:g.24240406_24240407del	GRCh38
NC_000014.8:g.24709612_24709613del , CM000676.1:g.24709612_24709613del	GRCh37
NC_000014.7:g.23779452_23779453del	NCBI36
NG_016650.1:g.7270_7271del
NG_054634.1:g.12990_12991del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1378_1379del
ENST00000557921.3:c.*10_*11del	ENSP00000453157.3:n.*10_*11del
ENST00000699682.1:n.1465_1466del
ENST00000699683.1:n.1515_1516del
ENST00000699684.1:c.*668_*669del	ENSP00000514523.1:n.*668_*669del
ENST00000699685.1:n.1279_1280del
ENST00000699686.1:c.*10_*11del	ENSP00000514524.1:n.*10_*11del
ENST00000699687.1:c.*10_*11del	ENSP00000514525.1:n.*10_*11del
ENST00000699688.1:n.1275_1276del
ENST00000699689.1:n.1631_1632del
ENST00000699690.1:n.1828_1829del
ENST00000699691.1:n.1972_1973del
ENST00000699693.1:n.1478+14_1478+15del
ENST00000699694.1:n.1734_1735del
ENST00000699695.1:c.*433+14_*433+15del	ENSP00000514526.1:n.*433+14_*433+15del
ENST00000699696.1:n.1378_1379del
ENST00000699697.1:c.1061+14_1061+15del	ENSP00000514527.1:n.1061+14_1061+15del
ENST00000699698.1:n.982+14_982+15del
ENST00000699699.1:n.1399_1400del
ENST00000699700.1:n.1522_1523del
ENST00000699701.1:c.*455_*456del	ENSP00000514528.1:n.*455_*456del
ENST00000267415.12:c.1061+14_1061+15del MANE Select	ENSP00000267415.7:n.1061+14_1061+15del
ENST00000646753.1:c.956+14_956+15del	ENSP00000494065.1:n.956+14_956+15del
ENST00000267415.11:c.1061+14_1061+15del	ENSP00000267415.7:n.1061+14_1061+15del
ENST00000399423.8:c.*10_*11del	ENSP00000382350.4:n.*10_*11del
ENST00000557915.1:n.194_195del
ENST00000558566.1:c.*447_*448del	ENSP00000453025.1:n.*447_*448del
ENST00000559969.5:c.833_834del
ENST00000560019.5:c.56+14_56+15del	ENSP00000453113.1:n.56+14_56+15del
ENST00000626689.2:c.*433+14_*433+15del	ENSP00000486681.1:n.*433+14_*433+15del
NM_001099274.1:c.1061+14_1061+15del	NP_001092744.1:n.1061+14_1061+15del
NM_012461.2:c.*10_*11del	NP_036593.2:n.*10_*11del
XM_005267528.2:c.1061+14_1061+15del	XP_005267585.1:n.1061+14_1061+15del
XM_005267529.2:c.956+14_956+15del	XP_005267586.1:n.956+14_956+15del
NM_001099274.2:c.1061+14_1061+15del	NP_001092744.1:n.1061+14_1061+15del
NM_001363668.1:c.956+14_956+15del	NP_001350597.1:n.956+14_956+15del
NM_012461.3:c.*10_*11del	NP_036593.2:n.*10_*11del
XM_011536642.2:c.*455_*456del	XP_011534944.1:n.*455_*456del
XM_017021216.2:c.419+14_419+15del	XP_016876705.1:n.419+14_419+15del
XM_017021217.1:c.419+14_419+15del	XP_016876706.1:n.419+14_419+15del
NM_001099274.3:c.1061+14_1061+15del MANE Select	NP_001092744.1:n.1061+14_1061+15del
NM_001363668.2:c.956+14_956+15del	NP_001350597.1:n.956+14_956+15del