Canonical Allele Identifier: CA919377173

Gene: TINF2

Linked Data

• dbSNP Id: rs1555303898

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240215del , CM000676.2:g.24240215del	GRCh38
NC_000014.8:g.24709421del , CM000676.1:g.24709421del	GRCh37
NC_000014.7:g.23779261del	NCBI36
NG_016650.1:g.7460del
NG_054634.1:g.12799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+48del
ENST00000557921.3:c.*200del	ENSP00000453157.3:n.*200del
ENST00000699682.1:n.1655del
ENST00000699683.1:n.1705del
ENST00000699684.1:c.*858del	ENSP00000514523.1:n.*858del
ENST00000699685.1:n.1469del
ENST00000699686.1:c.*200del	ENSP00000514524.1:n.*200del
ENST00000699687.1:c.*200del	ENSP00000514525.1:n.*200del
ENST00000699688.1:n.1465del
ENST00000699689.1:n.1821del
ENST00000699690.1:n.2018del
ENST00000699691.1:n.2162del
ENST00000699692.1:n.69-32del
ENST00000699693.1:n.1546+48del
ENST00000699694.1:n.1924del
ENST00000699695.1:c.*501+48del	ENSP00000514526.1:n.*501+48del
ENST00000699696.1:n.1520+48del
ENST00000699697.1:c.*40del	ENSP00000514527.1:n.*40del
ENST00000699698.1:n.1098del
ENST00000699699.1:n.1589del
ENST00000699700.1:n.1712del
ENST00000699701.1:c.*645del	ENSP00000514528.1:n.*645del
ENST00000267415.12:c.1129+48del MANE Select	ENSP00000267415.7:n.1129+48del
ENST00000646753.1:c.1024+48del	ENSP00000494065.1:n.1024+48del
ENST00000267415.11:c.1129+48del	ENSP00000267415.7:n.1129+48del
ENST00000399423.8:c.*200del	ENSP00000382350.4:n.*200del
ENST00000557915.1:n.336+48del
ENST00000558566.1:c.*637del	ENSP00000453025.1:n.*637del
ENST00000558703.1:n.28del
ENST00000559969.5:c.1023del
ENST00000560019.5:c.124+48del	ENSP00000453113.1:n.124+48del
ENST00000626689.2:c.*501+48del	ENSP00000486681.1:n.*501+48del
NM_001099274.1:c.1129+48del	NP_001092744.1:n.1129+48del
NM_012461.2:c.*200del	NP_036593.2:n.*200del
XM_005267528.2:c.1129+48del	XP_005267585.1:n.1129+48del
XM_005267529.2:c.1024+48del	XP_005267586.1:n.1024+48del
NM_001099274.2:c.1129+48del	NP_001092744.1:n.1129+48del
NM_001363668.1:c.1024+48del	NP_001350597.1:n.1024+48del
NM_012461.3:c.*200del	NP_036593.2:n.*200del
XM_011536642.2:c.*645del	XP_011534944.1:n.*645del
XM_017021216.2:c.487+48del	XP_016876705.1:n.487+48del
XM_017021217.1:c.487+48del	XP_016876706.1:n.487+48del
NM_001099274.3:c.1129+48del MANE Select	NP_001092744.1:n.1129+48del
NM_001363668.2:c.1024+48del	NP_001350597.1:n.1024+48del