Canonical Allele Identifier: CA485782077

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709786T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240580T>A , CM000676.2:g.24240580T>A	GRCh38
NC_000014.8:g.24709786T>A , CM000676.1:g.24709786T>A	GRCh37
NC_000014.7:g.23779626T>A	NCBI36
NG_016650.1:g.7095A>T
NG_054634.1:g.13164T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1203A>T
ENST00000557921.3:c.792A>T	ENSP00000453157.3:p.Ile264=
ENST00000699682.1:n.1290A>T
ENST00000699683.1:n.1340A>T
ENST00000699684.1:c.*493A>T	ENSP00000514523.1:n.*493A>T
ENST00000699685.1:n.1104A>T
ENST00000699686.1:c.693A>T	ENSP00000514524.1:p.Ile231=
ENST00000699687.1:c.795A>T	ENSP00000514525.1:p.Ile265=
ENST00000699688.1:n.1100A>T
ENST00000699689.1:n.1456A>T
ENST00000699690.1:n.1653A>T
ENST00000699691.1:n.1797A>T
ENST00000699693.1:n.1317A>T
ENST00000699694.1:n.1559A>T
ENST00000699695.1:c.*272A>T	ENSP00000514526.1:n.*272A>T
ENST00000699696.1:n.1203A>T
ENST00000699697.1:c.900A>T	ENSP00000514527.1:p.Ile300=
ENST00000699698.1:n.821A>T
ENST00000699699.1:n.1224A>T
ENST00000699700.1:n.1347A>T
ENST00000699701.1:c.*280A>T	ENSP00000514528.1:n.*280A>T
ENST00000267415.12:c.900A>T MANE Select	ENSP00000267415.7:p.Ile300=
ENST00000557921.2:c.792A>T	ENSP00000453157.2:p.Ile264=
ENST00000646753.1:c.795A>T	ENSP00000494065.1:p.Ile265=
ENST00000267415.11:c.900A>T	ENSP00000267415.7:p.Ile300=
ENST00000399423.8:c.900A>T	ENSP00000382350.4:p.Ile300=
ENST00000557915.1:n.19A>T
ENST00000558566.1:c.*272A>T	ENSP00000453025.1:n.*272A>T
ENST00000559019.1:c.*272A>T	ENSP00000453675.1:n.*272A>T
ENST00000559549.1:n.626A>T
ENST00000559969.5:c.758-100A>T
ENST00000626689.2:c.*272A>T	ENSP00000486681.1:n.*272A>T
NM_001099274.1:c.900A>T	NP_001092744.1:p.Ile300=
NM_012461.2:c.900A>T	NP_036593.2:p.Ile300=
XM_005267528.2:c.900A>T	XP_005267585.1:p.Ile300=
XM_005267529.2:c.795A>T	XP_005267586.1:p.Ile265=
NM_001099274.2:c.900A>T	NP_001092744.1:p.Ile300=
NM_001363668.1:c.795A>T	NP_001350597.1:p.Ile265=
NM_012461.3:c.900A>T	NP_036593.2:p.Ile300=
XM_011536642.2:c.*280A>T	XP_011534944.1:n.*280A>T
XM_017021216.2:c.258A>T	XP_016876705.1:p.Ile86=
XM_017021217.1:c.258A>T	XP_016876706.1:p.Ile86=
NM_001099274.3:c.900A>T MANE Select	NP_001092744.1:p.Ile300=
NM_001363668.2:c.795A>T	NP_001350597.1:p.Ile265=