Canonical Allele Identifier: CA2695213966

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240614_24240615del , CM000676.2:g.24240614_24240615del	GRCh38
NC_000014.8:g.24709820_24709821del , CM000676.1:g.24709820_24709821del	GRCh37
NC_000014.7:g.23779660_23779661del	NCBI36
NG_016650.1:g.7061_7062del
NG_054634.1:g.13198_13199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1169_1170del
ENST00000557921.3:c.758_759del	ENSP00000453157.3:p.Pro253LeufsTer2
ENST00000699682.1:n.1256_1257del
ENST00000699683.1:n.1306_1307del
ENST00000699684.1:c.*459_*460del	ENSP00000514523.1:n.*459_*460del
ENST00000699685.1:n.1070_1071del
ENST00000699686.1:c.659_660del	ENSP00000514524.1:p.Pro220LeufsTer2
ENST00000699687.1:c.761_762del	ENSP00000514525.1:p.Pro254LeufsTer2
ENST00000699688.1:n.1066_1067del
ENST00000699689.1:n.1422_1423del
ENST00000699690.1:n.1619_1620del
ENST00000699691.1:n.1763_1764del
ENST00000699693.1:n.1283_1284del
ENST00000699694.1:n.1525_1526del
ENST00000699695.1:c.*238_*239del	ENSP00000514526.1:n.*238_*239del
ENST00000699696.1:n.1169_1170del
ENST00000699697.1:c.866_867del	ENSP00000514527.1:p.Pro289LeufsTer2
ENST00000699698.1:n.787_788del
ENST00000699699.1:n.1190_1191del
ENST00000699700.1:n.1313_1314del
ENST00000699701.1:c.*246_*247del	ENSP00000514528.1:n.*246_*247del
ENST00000267415.12:c.866_867del MANE Select	ENSP00000267415.7:p.Pro289LeufsTer2
ENST00000557921.2:c.758_759del	ENSP00000453157.2:p.Pro253LeufsTer2
ENST00000646753.1:c.761_762del	ENSP00000494065.1:p.Pro254LeufsTer2
ENST00000267415.11:c.866_867del	ENSP00000267415.7:p.Pro289LeufsTer2
ENST00000399423.8:c.866_867del	ENSP00000382350.4:p.Pro289LeufsTer2
ENST00000558476.5:c.428_429del	ENSP00000452724.1:p.Pro143LeufsTer2
ENST00000558566.1:c.*238_*239del	ENSP00000453025.1:n.*238_*239del
ENST00000559019.1:c.*238_*239del	ENSP00000453675.1:n.*238_*239del
ENST00000559549.1:n.592_593del
ENST00000559969.5:c.757+65_757+66del
ENST00000626689.2:c.*238_*239del	ENSP00000486681.1:n.*238_*239del
NM_001099274.1:c.866_867del	NP_001092744.1:p.Pro289LeufsTer2
NM_012461.2:c.866_867del	NP_036593.2:p.Pro289LeufsTer2
XM_005267528.2:c.866_867del	XP_005267585.1:p.Pro289LeufsTer2
XM_005267529.2:c.761_762del	XP_005267586.1:p.Pro254LeufsTer2
NM_001099274.2:c.866_867del	NP_001092744.1:p.Pro289LeufsTer2
NM_001363668.1:c.761_762del	NP_001350597.1:p.Pro254LeufsTer2
NM_012461.3:c.866_867del	NP_036593.2:p.Pro289LeufsTer2
XM_011536642.2:c.*246_*247del	XP_011534944.1:n.*246_*247del
XM_017021216.2:c.224_225del	XP_016876705.1:p.Pro75LeufsTer2
XM_017021217.1:c.224_225del	XP_016876706.1:p.Pro75LeufsTer2
NM_001099274.3:c.866_867del MANE Select	NP_001092744.1:p.Pro289LeufsTer2
NM_001363668.2:c.761_762del	NP_001350597.1:p.Pro254LeufsTer2