Canonical Allele Identifier: CA2123849313

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240653_24240654delinsCT , CM000676.2:g.24240653_24240654delinsCT	GRCh38
NC_000014.8:g.24709859_24709860delinsCT , CM000676.1:g.24709859_24709860delinsCT	GRCh37
NC_000014.7:g.23779699_23779700delinsCT	NCBI36
NG_016650.1:g.7021_7022delinsAG
NG_054634.1:g.13237_13238delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1129_1130delinsAG
ENST00000557921.3:c.718_719delinsAG	ENSP00000453157.3:p.Arg240=
ENST00000699682.1:n.1216_1217delinsAG
ENST00000699683.1:n.1266_1267delinsAG
ENST00000699684.1:c.*419_*420delinsAG	ENSP00000514523.1:n.*419_*420delinsAG
ENST00000699685.1:n.1030_1031delinsAG
ENST00000699686.1:c.619_620delinsAG	ENSP00000514524.1:p.Arg207=
ENST00000699687.1:c.721_722delinsAG	ENSP00000514525.1:p.Arg241=
ENST00000699688.1:n.1026_1027delinsAG
ENST00000699689.1:n.1382_1383delinsAG
ENST00000699690.1:n.1579_1580delinsAG
ENST00000699691.1:n.1723_1724delinsAG
ENST00000699693.1:n.1243_1244delinsAG
ENST00000699694.1:n.1485_1486delinsAG
ENST00000699695.1:c.*198_*199delinsAG	ENSP00000514526.1:n.*198_*199delinsAG
ENST00000699696.1:n.1129_1130delinsAG
ENST00000699697.1:c.826_827delinsAG	ENSP00000514527.1:p.Arg276=
ENST00000699698.1:n.747_748delinsAG
ENST00000699699.1:n.1150_1151delinsAG
ENST00000699700.1:n.1273_1274delinsAG
ENST00000699701.1:c.*206_*207delinsAG	ENSP00000514528.1:n.*206_*207delinsAG
ENST00000267415.12:c.826_827delinsAG MANE Select	ENSP00000267415.7:p.Arg276=
ENST00000557921.2:c.718_719delinsAG	ENSP00000453157.2:p.Arg240=
ENST00000646753.1:c.721_722delinsAG	ENSP00000494065.1:p.Arg241=
ENST00000267415.11:c.826_827delinsAG	ENSP00000267415.7:p.Arg276=
ENST00000399423.8:c.826_827delinsAG	ENSP00000382350.4:p.Arg276=
ENST00000558476.5:c.388_389delinsAG	ENSP00000452724.1:p.Arg130=
ENST00000558566.1:c.*198_*199delinsAG	ENSP00000453025.1:n.*198_*199delinsAG
ENST00000559019.1:c.*198_*199delinsAG	ENSP00000453675.1:n.*198_*199delinsAG
ENST00000559549.1:n.552_553delinsAG
ENST00000559969.5:c.757+25_757+26delinsAG
ENST00000626689.2:c.*198_*199delinsAG	ENSP00000486681.1:n.*198_*199delinsAG
NM_001099274.1:c.826_827delinsAG	NP_001092744.1:p.Arg276=
NM_012461.2:c.826_827delinsAG	NP_036593.2:p.Arg276=
XM_005267528.2:c.826_827delinsAG	XP_005267585.1:p.Arg276=
XM_005267529.2:c.721_722delinsAG	XP_005267586.1:p.Arg241=
NM_001099274.2:c.826_827delinsAG	NP_001092744.1:p.Arg276=
NM_001363668.1:c.721_722delinsAG	NP_001350597.1:p.Arg241=
NM_012461.3:c.826_827delinsAG	NP_036593.2:p.Arg276=
XM_011536642.2:c.*206_*207delinsAG	XP_011534944.1:n.*206_*207delinsAG
XM_017021216.2:c.184_185delinsAG	XP_016876705.1:p.Arg62=
XM_017021217.1:c.184_185delinsAG	XP_016876706.1:p.Arg62=
NM_001099274.3:c.826_827delinsAG MANE Select	NP_001092744.1:p.Arg276=
NM_001363668.2:c.721_722delinsAG	NP_001350597.1:p.Arg241=