Canonical Allele Identifier: CA2123849283

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240587_24240588delinsTG , CM000676.2:g.24240587_24240588delinsTG	GRCh38
NC_000014.8:g.24709793_24709794delinsTG , CM000676.1:g.24709793_24709794delinsTG	GRCh37
NC_000014.7:g.23779633_23779634delinsTG	NCBI36
NG_016650.1:g.7087_7088delinsCA
NG_054634.1:g.13171_13172delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1195_1196delinsCA
ENST00000557921.3:c.784_785delinsCA	ENSP00000453157.3:p.Gln262=
ENST00000699682.1:n.1282_1283delinsCA
ENST00000699683.1:n.1332_1333delinsCA
ENST00000699684.1:c.*485_*486delinsCA	ENSP00000514523.1:n.*485_*486delinsCA
ENST00000699685.1:n.1096_1097delinsCA
ENST00000699686.1:c.685_686delinsCA	ENSP00000514524.1:p.Gln229=
ENST00000699687.1:c.787_788delinsCA	ENSP00000514525.1:p.Gln263=
ENST00000699688.1:n.1092_1093delinsCA
ENST00000699689.1:n.1448_1449delinsCA
ENST00000699690.1:n.1645_1646delinsCA
ENST00000699691.1:n.1789_1790delinsCA
ENST00000699693.1:n.1309_1310delinsCA
ENST00000699694.1:n.1551_1552delinsCA
ENST00000699695.1:c.*264_*265delinsCA	ENSP00000514526.1:n.*264_*265delinsCA
ENST00000699696.1:n.1195_1196delinsCA
ENST00000699697.1:c.892_893delinsCA	ENSP00000514527.1:p.Gln298=
ENST00000699698.1:n.813_814delinsCA
ENST00000699699.1:n.1216_1217delinsCA
ENST00000699700.1:n.1339_1340delinsCA
ENST00000699701.1:c.*272_*273delinsCA	ENSP00000514528.1:n.*272_*273delinsCA
ENST00000267415.12:c.892_893delinsCA MANE Select	ENSP00000267415.7:p.Gln298=
ENST00000557921.2:c.784_785delinsCA	ENSP00000453157.2:p.Gln262=
ENST00000646753.1:c.787_788delinsCA	ENSP00000494065.1:p.Gln263=
ENST00000267415.11:c.892_893delinsCA	ENSP00000267415.7:p.Gln298=
ENST00000399423.8:c.892_893delinsCA	ENSP00000382350.4:p.Gln298=
ENST00000557915.1:n.11_12delinsCA
ENST00000558566.1:c.*264_*265delinsCA	ENSP00000453025.1:n.*264_*265delinsCA
ENST00000559019.1:c.*264_*265delinsCA	ENSP00000453675.1:n.*264_*265delinsCA
ENST00000559549.1:n.618_619delinsCA
ENST00000559969.5:c.757+91_757+92delinsCA
ENST00000626689.2:c.*264_*265delinsCA	ENSP00000486681.1:n.*264_*265delinsCA
NM_001099274.1:c.892_893delinsCA	NP_001092744.1:p.Gln298=
NM_012461.2:c.892_893delinsCA	NP_036593.2:p.Gln298=
XM_005267528.2:c.892_893delinsCA	XP_005267585.1:p.Gln298=
XM_005267529.2:c.787_788delinsCA	XP_005267586.1:p.Gln263=
NM_001099274.2:c.892_893delinsCA	NP_001092744.1:p.Gln298=
NM_001363668.1:c.787_788delinsCA	NP_001350597.1:p.Gln263=
NM_012461.3:c.892_893delinsCA	NP_036593.2:p.Gln298=
XM_011536642.2:c.*272_*273delinsCA	XP_011534944.1:n.*272_*273delinsCA
XM_017021216.2:c.250_251delinsCA	XP_016876705.1:p.Gln84=
XM_017021217.1:c.250_251delinsCA	XP_016876706.1:p.Gln84=
NM_001099274.3:c.892_893delinsCA MANE Select	NP_001092744.1:p.Gln298=
NM_001363668.2:c.787_788delinsCA	NP_001350597.1:p.Gln263=