Canonical Allele Identifier: CA2624345075

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240186-ACTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240189_24240191del , CM000676.2:g.24240189_24240191del	GRCh38
NC_000014.8:g.24709395_24709397del , CM000676.1:g.24709395_24709397del	GRCh37
NC_000014.7:g.23779235_23779237del	NCBI36
NG_016650.1:g.7486_7488del
NG_054634.1:g.12773_12775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1521-34_1521-32del
ENST00000557921.3:c.*226_*228del	ENSP00000453157.3:n.*226_*228del
ENST00000699682.1:n.1681_1683del
ENST00000699683.1:n.1731_1733del
ENST00000699684.1:c.*884_*886del	ENSP00000514523.1:n.*884_*886del
ENST00000699685.1:n.1495_1497del
ENST00000699686.1:c.*226_*228del	ENSP00000514524.1:n.*226_*228del
ENST00000699687.1:c.*226_*228del	ENSP00000514525.1:n.*226_*228del
ENST00000699688.1:n.1491_1493del
ENST00000699689.1:n.1847_1849del
ENST00000699690.1:n.2044_2046del
ENST00000699691.1:n.2188_2190del
ENST00000699692.1:n.69-6_69-4del
ENST00000699693.1:n.1547-34_1547-32del
ENST00000699694.1:n.1950_1952del
ENST00000699695.1:c.*502-34_*502-32del	ENSP00000514526.1:n.*502-34_*502-32del
ENST00000699696.1:n.1521-34_1521-32del
ENST00000699697.1:c.*66_*68del	ENSP00000514527.1:n.*66_*68del
ENST00000699698.1:n.1124_1126del
ENST00000699699.1:n.1615_1617del
ENST00000699700.1:n.1738_1740del
ENST00000699701.1:c.*671_*673del	ENSP00000514528.1:n.*671_*673del
ENST00000267415.12:c.1130-34_1130-32del MANE Select	ENSP00000267415.7:n.1130-34_1130-32del
ENST00000646753.1:c.1025-34_1025-32del	ENSP00000494065.1:n.1025-34_1025-32del
ENST00000267415.11:c.1130-34_1130-32del	ENSP00000267415.7:n.1130-34_1130-32del
ENST00000399423.8:c.*226_*228del	ENSP00000382350.4:n.*226_*228del
ENST00000557915.1:n.337-34_337-32del
ENST00000558566.1:c.*663_*665del	ENSP00000453025.1:n.*663_*665del
ENST00000558703.1:n.54_56del
ENST00000559969.5:c.1049_1051del
ENST00000560019.5:c.125-34_125-32del	ENSP00000453113.1:n.125-34_125-32del
ENST00000626689.2:c.*502-34_*502-32del	ENSP00000486681.1:n.*502-34_*502-32del
NM_001099274.1:c.1130-34_1130-32del	NP_001092744.1:n.1130-34_1130-32del
NM_012461.2:c.*226_*228del	NP_036593.2:n.*226_*228del
XM_005267528.2:c.1130-34_1130-32del	XP_005267585.1:n.1130-34_1130-32del
XM_005267529.2:c.1025-34_1025-32del	XP_005267586.1:n.1025-34_1025-32del
NM_001099274.2:c.1130-34_1130-32del	NP_001092744.1:n.1130-34_1130-32del
NM_001363668.1:c.1025-34_1025-32del	NP_001350597.1:n.1025-34_1025-32del
NM_012461.3:c.*226_*228del	NP_036593.2:n.*226_*228del
XM_011536642.2:c.*671_*673del	XP_011534944.1:n.*671_*673del
XM_017021216.2:c.488-34_488-32del	XP_016876705.1:n.488-34_488-32del
XM_017021217.1:c.488-34_488-32del	XP_016876706.1:n.488-34_488-32del
NM_001099274.3:c.1130-34_1130-32del MANE Select	NP_001092744.1:n.1130-34_1130-32del
NM_001363668.2:c.1025-34_1025-32del	NP_001350597.1:n.1025-34_1025-32del