Canonical Allele Identifier: CA2624345073

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240182-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240182T>A , CM000676.2:g.24240182T>A	GRCh38
NC_000014.8:g.24709388T>A , CM000676.1:g.24709388T>A	GRCh37
NC_000014.7:g.23779228T>A	NCBI36
NG_016650.1:g.7493A>T
NG_054634.1:g.12766T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1521-27A>T
ENST00000557921.3:c.*233A>T	ENSP00000453157.3:n.*233A>T
ENST00000699682.1:n.1688A>T
ENST00000699683.1:n.1738A>T
ENST00000699684.1:c.*891A>T	ENSP00000514523.1:n.*891A>T
ENST00000699685.1:n.1502A>T
ENST00000699686.1:c.*233A>T	ENSP00000514524.1:n.*233A>T
ENST00000699687.1:c.*233A>T	ENSP00000514525.1:n.*233A>T
ENST00000699688.1:n.1498A>T
ENST00000699689.1:n.1854A>T
ENST00000699690.1:n.2051A>T
ENST00000699691.1:n.2195A>T
ENST00000699692.1:n.70A>T
ENST00000699693.1:n.1547-27A>T
ENST00000699694.1:n.1957A>T
ENST00000699695.1:c.*502-27A>T	ENSP00000514526.1:n.*502-27A>T
ENST00000699696.1:n.1521-27A>T
ENST00000699697.1:c.*73A>T	ENSP00000514527.1:n.*73A>T
ENST00000699698.1:n.1131A>T
ENST00000699699.1:n.1622A>T
ENST00000699700.1:n.1745A>T
ENST00000699701.1:c.*678A>T	ENSP00000514528.1:n.*678A>T
ENST00000267415.12:c.1130-27A>T MANE Select	ENSP00000267415.7:n.1130-27A>T
ENST00000646753.1:c.1025-27A>T	ENSP00000494065.1:n.1025-27A>T
ENST00000267415.11:c.1130-27A>T	ENSP00000267415.7:n.1130-27A>T
ENST00000399423.8:c.*233A>T	ENSP00000382350.4:n.*233A>T
ENST00000557915.1:n.337-27A>T
ENST00000558566.1:c.*670A>T	ENSP00000453025.1:n.*670A>T
ENST00000558703.1:n.61A>T
ENST00000559969.5:c.1056A>T
ENST00000560019.5:c.125-27A>T	ENSP00000453113.1:n.125-27A>T
ENST00000626689.2:c.*502-27A>T	ENSP00000486681.1:n.*502-27A>T
NM_001099274.1:c.1130-27A>T	NP_001092744.1:n.1130-27A>T
NM_012461.2:c.*233A>T	NP_036593.2:n.*233A>T
XM_005267528.2:c.1130-27A>T	XP_005267585.1:n.1130-27A>T
XM_005267529.2:c.1025-27A>T	XP_005267586.1:n.1025-27A>T
NM_001099274.2:c.1130-27A>T	NP_001092744.1:n.1130-27A>T
NM_001363668.1:c.1025-27A>T	NP_001350597.1:n.1025-27A>T
NM_012461.3:c.*233A>T	NP_036593.2:n.*233A>T
XM_011536642.2:c.*678A>T	XP_011534944.1:n.*678A>T
XM_017021216.2:c.488-27A>T	XP_016876705.1:n.488-27A>T
XM_017021217.1:c.488-27A>T	XP_016876706.1:n.488-27A>T
NM_001099274.3:c.1130-27A>T MANE Select	NP_001092744.1:n.1130-27A>T
NM_001363668.2:c.1025-27A>T	NP_001350597.1:n.1025-27A>T