Canonical Allele Identifier: CA2695213964

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240606_24240609del , CM000676.2:g.24240606_24240609del	GRCh38
NC_000014.8:g.24709812_24709815del , CM000676.1:g.24709812_24709815del	GRCh37
NC_000014.7:g.23779652_23779655del	NCBI36
NG_016650.1:g.7067_7070del
NG_054634.1:g.13190_13193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1175_1178del
ENST00000557921.3:c.764_767del	ENSP00000453157.3:p.Arg255IlefsTer25
ENST00000699682.1:n.1262_1265del
ENST00000699683.1:n.1312_1315del
ENST00000699684.1:c.*465_*468del	ENSP00000514523.1:n.*465_*468del
ENST00000699685.1:n.1076_1079del
ENST00000699686.1:c.665_668del	ENSP00000514524.1:p.Arg222IlefsTer25
ENST00000699687.1:c.767_770del	ENSP00000514525.1:p.Arg256IlefsTer25
ENST00000699688.1:n.1072_1075del
ENST00000699689.1:n.1428_1431del
ENST00000699690.1:n.1625_1628del
ENST00000699691.1:n.1769_1772del
ENST00000699693.1:n.1289_1292del
ENST00000699694.1:n.1531_1534del
ENST00000699695.1:c.*244_*247del	ENSP00000514526.1:n.*244_*247del
ENST00000699696.1:n.1175_1178del
ENST00000699697.1:c.872_875del	ENSP00000514527.1:p.Arg291IlefsTer25
ENST00000699698.1:n.793_796del
ENST00000699699.1:n.1196_1199del
ENST00000699700.1:n.1319_1322del
ENST00000699701.1:c.*252_*255del	ENSP00000514528.1:n.*252_*255del
ENST00000267415.12:c.872_875del MANE Select	ENSP00000267415.7:p.Arg291IlefsTer25
ENST00000557921.2:c.764_767del	ENSP00000453157.2:p.Arg255IlefsTer25
ENST00000646753.1:c.767_770del	ENSP00000494065.1:p.Arg256IlefsTer25
ENST00000267415.11:c.872_875del	ENSP00000267415.7:p.Arg291IlefsTer25
ENST00000399423.8:c.872_875del	ENSP00000382350.4:p.Arg291IlefsTer25
ENST00000558476.5:c.434_437del	ENSP00000452724.1:p.Arg145IlefsTer?
ENST00000558566.1:c.*244_*247del	ENSP00000453025.1:n.*244_*247del
ENST00000559019.1:c.*244_*247del	ENSP00000453675.1:n.*244_*247del
ENST00000559549.1:n.598_601del
ENST00000559969.5:c.757+71_757+74del
ENST00000626689.2:c.*244_*247del	ENSP00000486681.1:n.*244_*247del
NM_001099274.1:c.872_875del	NP_001092744.1:p.Arg291IlefsTer25
NM_012461.2:c.872_875del	NP_036593.2:p.Arg291IlefsTer25
XM_005267528.2:c.872_875del	XP_005267585.1:p.Arg291IlefsTer25
XM_005267529.2:c.767_770del	XP_005267586.1:p.Arg256IlefsTer25
NM_001099274.2:c.872_875del	NP_001092744.1:p.Arg291IlefsTer25
NM_001363668.1:c.767_770del	NP_001350597.1:p.Arg256IlefsTer25
NM_012461.3:c.872_875del	NP_036593.2:p.Arg291IlefsTer25
XM_011536642.2:c.*252_*255del	XP_011534944.1:n.*252_*255del
XM_017021216.2:c.230_233del	XP_016876705.1:p.Arg77IlefsTer25
XM_017021217.1:c.230_233del	XP_016876706.1:p.Arg77IlefsTer25
NM_001099274.3:c.872_875del MANE Select	NP_001092744.1:p.Arg291IlefsTer25
NM_001363668.2:c.767_770del	NP_001350597.1:p.Arg256IlefsTer25