Canonical Allele Identifier: CA2575493627

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240400G>A , CM000676.2:g.24240400G>A	GRCh38
NC_000014.8:g.24709606G>A , CM000676.1:g.24709606G>A	GRCh37
NC_000014.7:g.23779446G>A	NCBI36
NG_016650.1:g.7275C>T
NG_054634.1:g.12984G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1383C>T
ENST00000557921.3:c.*15C>T	ENSP00000453157.3:n.*15C>T
ENST00000699682.1:n.1470C>T
ENST00000699683.1:n.1520C>T
ENST00000699684.1:c.*673C>T	ENSP00000514523.1:n.*673C>T
ENST00000699685.1:n.1284C>T
ENST00000699686.1:c.*15C>T	ENSP00000514524.1:n.*15C>T
ENST00000699687.1:c.*15C>T	ENSP00000514525.1:n.*15C>T
ENST00000699688.1:n.1280C>T
ENST00000699689.1:n.1636C>T
ENST00000699690.1:n.1833C>T
ENST00000699691.1:n.1977C>T
ENST00000699693.1:n.1478+19C>T
ENST00000699694.1:n.1739C>T
ENST00000699695.1:c.*433+19C>T	ENSP00000514526.1:n.*433+19C>T
ENST00000699696.1:n.1383C>T
ENST00000699697.1:c.1061+19C>T	ENSP00000514527.1:n.1061+19C>T
ENST00000699698.1:n.982+19C>T
ENST00000699699.1:n.1404C>T
ENST00000699700.1:n.1527C>T
ENST00000699701.1:c.*460C>T	ENSP00000514528.1:n.*460C>T
ENST00000267415.12:c.1061+19C>T MANE Select	ENSP00000267415.7:n.1061+19C>T
ENST00000646753.1:c.956+19C>T	ENSP00000494065.1:n.956+19C>T
ENST00000267415.11:c.1061+19C>T	ENSP00000267415.7:n.1061+19C>T
ENST00000399423.8:c.*15C>T	ENSP00000382350.4:n.*15C>T
ENST00000557915.1:n.199C>T
ENST00000558566.1:c.*452C>T	ENSP00000453025.1:n.*452C>T
ENST00000559969.5:c.838C>T
ENST00000560019.5:c.56+19C>T	ENSP00000453113.1:n.56+19C>T
ENST00000626689.2:c.*433+19C>T	ENSP00000486681.1:n.*433+19C>T
NM_001099274.1:c.1061+19C>T	NP_001092744.1:n.1061+19C>T
NM_012461.2:c.*15C>T	NP_036593.2:n.*15C>T
XM_005267528.2:c.1061+19C>T	XP_005267585.1:n.1061+19C>T
XM_005267529.2:c.956+19C>T	XP_005267586.1:n.956+19C>T
NM_001099274.2:c.1061+19C>T	NP_001092744.1:n.1061+19C>T
NM_001363668.1:c.956+19C>T	NP_001350597.1:n.956+19C>T
NM_012461.3:c.*15C>T	NP_036593.2:n.*15C>T
XM_011536642.2:c.*460C>T	XP_011534944.1:n.*460C>T
XM_017021216.2:c.419+19C>T	XP_016876705.1:n.419+19C>T
XM_017021217.1:c.419+19C>T	XP_016876706.1:n.419+19C>T
NM_001099274.3:c.1061+19C>T MANE Select	NP_001092744.1:n.1061+19C>T
NM_001363668.2:c.956+19C>T	NP_001350597.1:n.956+19C>T