Canonical Allele Identifier: CA2123849326

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240678_24240681delinsCTCT , CM000676.2:g.24240678_24240681delinsCTCT	GRCh38
NC_000014.8:g.24709884_24709887delinsCTCT , CM000676.1:g.24709884_24709887delinsCTCT	GRCh37
NC_000014.7:g.23779724_23779727delinsCTCT	NCBI36
NG_016650.1:g.6994_6997delinsAGAG
NG_054634.1:g.13262_13265delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1102_1105delinsAGAG
ENST00000557921.3:c.691_694delinsAGAG	ENSP00000453157.3:p.Arg231=
ENST00000699682.1:n.1189_1192delinsAGAG
ENST00000699683.1:n.1239_1242delinsAGAG
ENST00000699684.1:c.*392_*395delinsAGAG	ENSP00000514523.1:n.*392_*395delinsAGAG
ENST00000699685.1:n.1003_1006delinsAGAG
ENST00000699686.1:c.592_595delinsAGAG	ENSP00000514524.1:p.Arg198=
ENST00000699687.1:c.694_697delinsAGAG	ENSP00000514525.1:p.Arg232=
ENST00000699688.1:n.999_1002delinsAGAG
ENST00000699689.1:n.1355_1358delinsAGAG
ENST00000699690.1:n.1552_1555delinsAGAG
ENST00000699691.1:n.1696_1699delinsAGAG
ENST00000699693.1:n.1216_1219delinsAGAG
ENST00000699694.1:n.1458_1461delinsAGAG
ENST00000699695.1:c.*171_*174delinsAGAG	ENSP00000514526.1:n.*171_*174delinsAGAG
ENST00000699696.1:n.1102_1105delinsAGAG
ENST00000699697.1:c.799_802delinsAGAG	ENSP00000514527.1:p.Arg267=
ENST00000699698.1:n.720_723delinsAGAG
ENST00000699699.1:n.1123_1126delinsAGAG
ENST00000699700.1:n.1246_1249delinsAGAG
ENST00000699701.1:c.*179_*182delinsAGAG	ENSP00000514528.1:n.*179_*182delinsAGAG
ENST00000267415.12:c.799_802delinsAGAG MANE Select	ENSP00000267415.7:p.Arg267=
ENST00000557921.2:c.691_694delinsAGAG	ENSP00000453157.2:p.Arg231=
ENST00000646753.1:c.694_697delinsAGAG	ENSP00000494065.1:p.Arg232=
ENST00000267415.11:c.799_802delinsAGAG	ENSP00000267415.7:p.Arg267=
ENST00000399423.8:c.799_802delinsAGAG	ENSP00000382350.4:p.Arg267=
ENST00000558476.5:c.361_364delinsAGAG	ENSP00000452724.1:p.Arg121=
ENST00000558566.1:c.*171_*174delinsAGAG	ENSP00000453025.1:n.*171_*174delinsAGAG
ENST00000559019.1:c.*171_*174delinsAGAG	ENSP00000453675.1:n.*171_*174delinsAGAG
ENST00000559549.1:n.525_528delinsAGAG
ENST00000559969.5:c.755_757+1delinsAGAG
ENST00000626689.2:c.*171_*174delinsAGAG	ENSP00000486681.1:n.*171_*174delinsAGAG
NM_001099274.1:c.799_802delinsAGAG	NP_001092744.1:p.Arg267=
NM_012461.2:c.799_802delinsAGAG	NP_036593.2:p.Arg267=
XM_005267528.2:c.799_802delinsAGAG	XP_005267585.1:p.Arg267=
XM_005267529.2:c.694_697delinsAGAG	XP_005267586.1:p.Arg232=
NM_001099274.2:c.799_802delinsAGAG	NP_001092744.1:p.Arg267=
NM_001363668.1:c.694_697delinsAGAG	NP_001350597.1:p.Arg232=
NM_012461.3:c.799_802delinsAGAG	NP_036593.2:p.Arg267=
XM_011536642.2:c.*179_*182delinsAGAG	XP_011534944.1:n.*179_*182delinsAGAG
XM_017021216.2:c.157_160delinsAGAG	XP_016876705.1:p.Arg53=
XM_017021217.1:c.157_160delinsAGAG	XP_016876706.1:p.Arg53=
NM_001099274.3:c.799_802delinsAGAG MANE Select	NP_001092744.1:p.Arg267=
NM_001363668.2:c.694_697delinsAGAG	NP_001350597.1:p.Arg232=