Canonical Allele Identifier: CA485782024

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709497T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240291T>A , CM000676.2:g.24240291T>A	GRCh38
NC_000014.8:g.24709497T>A , CM000676.1:g.24709497T>A	GRCh37
NC_000014.7:g.23779337T>A	NCBI36
NG_016650.1:g.7384A>T
NG_054634.1:g.12875T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1492A>T
ENST00000557921.3:c.*124A>T	ENSP00000453157.3:n.*124A>T
ENST00000699682.1:n.1579A>T
ENST00000699683.1:n.1629A>T
ENST00000699684.1:c.*782A>T	ENSP00000514523.1:n.*782A>T
ENST00000699685.1:n.1393A>T
ENST00000699686.1:c.*124A>T	ENSP00000514524.1:n.*124A>T
ENST00000699687.1:c.*124A>T	ENSP00000514525.1:n.*124A>T
ENST00000699688.1:n.1389A>T
ENST00000699689.1:n.1745A>T
ENST00000699690.1:n.1942A>T
ENST00000699691.1:n.2086A>T
ENST00000699692.1:n.40A>T
ENST00000699693.1:n.1518A>T
ENST00000699694.1:n.1848A>T
ENST00000699695.1:c.*473A>T	ENSP00000514526.1:n.*473A>T
ENST00000699696.1:n.1492A>T
ENST00000699697.1:c.1101A>T	ENSP00000514527.1:p.Ser367=
ENST00000699698.1:n.1022A>T
ENST00000699699.1:n.1513A>T
ENST00000699700.1:n.1636A>T
ENST00000699701.1:c.*569A>T	ENSP00000514528.1:n.*569A>T
ENST00000267415.12:c.1101A>T MANE Select	ENSP00000267415.7:p.Ser367=
ENST00000646753.1:c.996A>T	ENSP00000494065.1:p.Ser332=
ENST00000267415.11:c.1101A>T	ENSP00000267415.7:p.Ser367=
ENST00000399423.8:c.*124A>T	ENSP00000382350.4:n.*124A>T
ENST00000557915.1:n.308A>T
ENST00000558566.1:c.*561A>T	ENSP00000453025.1:n.*561A>T
ENST00000559969.5:c.947A>T
ENST00000560019.5:c.96A>T	ENSP00000453113.1:p.Ser32=
ENST00000626689.2:c.*473A>T	ENSP00000486681.1:n.*473A>T
NM_001099274.1:c.1101A>T	NP_001092744.1:p.Ser367=
NM_012461.2:c.*124A>T	NP_036593.2:n.*124A>T
XM_005267528.2:c.1101A>T	XP_005267585.1:p.Ser367=
XM_005267529.2:c.996A>T	XP_005267586.1:p.Ser332=
NM_001099274.2:c.1101A>T	NP_001092744.1:p.Ser367=
NM_001363668.1:c.996A>T	NP_001350597.1:p.Ser332=
NM_012461.3:c.*124A>T	NP_036593.2:n.*124A>T
XM_011536642.2:c.*569A>T	XP_011534944.1:n.*569A>T
XM_017021216.2:c.459A>T	XP_016876705.1:p.Ser153=
XM_017021217.1:c.459A>T	XP_016876706.1:p.Ser153=
NM_001099274.3:c.1101A>T MANE Select	NP_001092744.1:p.Ser367=
NM_001363668.2:c.996A>T	NP_001350597.1:p.Ser332=