Canonical Allele Identifier: CA2624345071

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240178-AAACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240180_24240183del , CM000676.2:g.24240180_24240183del	GRCh38
NC_000014.8:g.24709386_24709389del , CM000676.1:g.24709386_24709389del	GRCh37
NC_000014.7:g.23779226_23779229del	NCBI36
NG_016650.1:g.7493_7496del
NG_054634.1:g.12764_12767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1521-27_1521-24del
ENST00000557921.3:c.*233_*236del	ENSP00000453157.3:n.*233_*236del
ENST00000699682.1:n.1688_1691del
ENST00000699683.1:n.1738_1741del
ENST00000699684.1:c.*891_*894del	ENSP00000514523.1:n.*891_*894del
ENST00000699685.1:n.1502_1505del
ENST00000699686.1:c.*233_*236del	ENSP00000514524.1:n.*233_*236del
ENST00000699687.1:c.*233_*236del	ENSP00000514525.1:n.*233_*236del
ENST00000699688.1:n.1498_1501del
ENST00000699689.1:n.1854_1857del
ENST00000699690.1:n.2051_2054del
ENST00000699691.1:n.2195_2198del
ENST00000699692.1:n.70_73del
ENST00000699693.1:n.1547-27_1547-24del
ENST00000699694.1:n.1957_1960del
ENST00000699695.1:c.*502-27_*502-24del	ENSP00000514526.1:n.*502-27_*502-24del
ENST00000699696.1:n.1521-27_1521-24del
ENST00000699697.1:c.*73_*76del	ENSP00000514527.1:n.*73_*76del
ENST00000699698.1:n.1131_1134del
ENST00000699699.1:n.1622_1625del
ENST00000699700.1:n.1745_1748del
ENST00000699701.1:c.*678_*681del	ENSP00000514528.1:n.*678_*681del
ENST00000267415.12:c.1130-27_1130-24del MANE Select	ENSP00000267415.7:n.1130-27_1130-24del
ENST00000646753.1:c.1025-27_1025-24del	ENSP00000494065.1:n.1025-27_1025-24del
ENST00000267415.11:c.1130-27_1130-24del	ENSP00000267415.7:n.1130-27_1130-24del
ENST00000399423.8:c.*233_*236del	ENSP00000382350.4:n.*233_*236del
ENST00000557915.1:n.337-27_337-24del
ENST00000558566.1:c.*670_*673del	ENSP00000453025.1:n.*670_*673del
ENST00000558703.1:n.61_64del
ENST00000559969.5:c.1056_1059del
ENST00000560019.5:c.125-27_125-24del	ENSP00000453113.1:n.125-27_125-24del
ENST00000626689.2:c.*502-27_*502-24del	ENSP00000486681.1:n.*502-27_*502-24del
NM_001099274.1:c.1130-27_1130-24del	NP_001092744.1:n.1130-27_1130-24del
NM_012461.2:c.*233_*236del	NP_036593.2:n.*233_*236del
XM_005267528.2:c.1130-27_1130-24del	XP_005267585.1:n.1130-27_1130-24del
XM_005267529.2:c.1025-27_1025-24del	XP_005267586.1:n.1025-27_1025-24del
NM_001099274.2:c.1130-27_1130-24del	NP_001092744.1:n.1130-27_1130-24del
NM_001363668.1:c.1025-27_1025-24del	NP_001350597.1:n.1025-27_1025-24del
NM_012461.3:c.*233_*236del	NP_036593.2:n.*233_*236del
XM_011536642.2:c.*678_*681del	XP_011534944.1:n.*678_*681del
XM_017021216.2:c.488-27_488-24del	XP_016876705.1:n.488-27_488-24del
XM_017021217.1:c.488-27_488-24del	XP_016876706.1:n.488-27_488-24del
NM_001099274.3:c.1130-27_1130-24del MANE Select	NP_001092744.1:n.1130-27_1130-24del
NM_001363668.2:c.1025-27_1025-24del	NP_001350597.1:n.1025-27_1025-24del