Canonical Allele Identifier: CA2123849191

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240469_24240470delinsTC , CM000676.2:g.24240469_24240470delinsTC	GRCh38
NC_000014.8:g.24709675_24709676delinsTC , CM000676.1:g.24709675_24709676delinsTC	GRCh37
NC_000014.7:g.23779515_23779516delinsTC	NCBI36
NG_016650.1:g.7205_7206delinsGA
NG_054634.1:g.13053_13054delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1313_1314delinsGA
ENST00000557921.3:c.902_903delinsGA	ENSP00000453157.3:p.Gly301=
ENST00000699682.1:n.1400_1401delinsGA
ENST00000699683.1:n.1450_1451delinsGA
ENST00000699684.1:c.*603_*604delinsGA	ENSP00000514523.1:n.*603_*604delinsGA
ENST00000699685.1:n.1214_1215delinsGA
ENST00000699686.1:c.803_804delinsGA	ENSP00000514524.1:p.Gly268=
ENST00000699687.1:c.905_906delinsGA	ENSP00000514525.1:p.Gly302=
ENST00000699688.1:n.1210_1211delinsGA
ENST00000699689.1:n.1566_1567delinsGA
ENST00000699690.1:n.1763_1764delinsGA
ENST00000699691.1:n.1907_1908delinsGA
ENST00000699693.1:n.1427_1428delinsGA
ENST00000699694.1:n.1669_1670delinsGA
ENST00000699695.1:c.*382_*383delinsGA	ENSP00000514526.1:n.*382_*383delinsGA
ENST00000699696.1:n.1313_1314delinsGA
ENST00000699697.1:c.1010_1011delinsGA	ENSP00000514527.1:p.Gly337=
ENST00000699698.1:n.931_932delinsGA
ENST00000699699.1:n.1334_1335delinsGA
ENST00000699700.1:n.1457_1458delinsGA
ENST00000699701.1:c.*390_*391delinsGA	ENSP00000514528.1:n.*390_*391delinsGA
ENST00000267415.12:c.1010_1011delinsGA MANE Select	ENSP00000267415.7:p.Gly337=
ENST00000646753.1:c.905_906delinsGA	ENSP00000494065.1:p.Gly302=
ENST00000267415.11:c.1010_1011delinsGA	ENSP00000267415.7:p.Gly337=
ENST00000399423.8:c.1010_1011delinsGA	ENSP00000382350.4:p.Gly337=
ENST00000557915.1:n.129_130delinsGA
ENST00000558566.1:c.*382_*383delinsGA	ENSP00000453025.1:n.*382_*383delinsGA
ENST00000559969.5:c.768_769delinsGA
ENST00000560019.5:c.5_6delinsGA	ENSP00000453113.1:p.Gly2=
ENST00000626689.2:c.*382_*383delinsGA	ENSP00000486681.1:n.*382_*383delinsGA
NM_001099274.1:c.1010_1011delinsGA	NP_001092744.1:p.Gly337=
NM_012461.2:c.1010_1011delinsGA	NP_036593.2:p.Gly337=
XM_005267528.2:c.1010_1011delinsGA	XP_005267585.1:p.Gly337=
XM_005267529.2:c.905_906delinsGA	XP_005267586.1:p.Gly302=
NM_001099274.2:c.1010_1011delinsGA	NP_001092744.1:p.Gly337=
NM_001363668.1:c.905_906delinsGA	NP_001350597.1:p.Gly302=
NM_012461.3:c.1010_1011delinsGA	NP_036593.2:p.Gly337=
XM_011536642.2:c.*390_*391delinsGA	XP_011534944.1:n.*390_*391delinsGA
XM_017021216.2:c.368_369delinsGA	XP_016876705.1:p.Gly123=
XM_017021217.1:c.368_369delinsGA	XP_016876706.1:p.Gly123=
NM_001099274.3:c.1010_1011delinsGA MANE Select	NP_001092744.1:p.Gly337=
NM_001363668.2:c.905_906delinsGA	NP_001350597.1:p.Gly302=