Canonical Allele Identifier: CA389223337

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709628T>A (hg19) ; chr14:g.24240422T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240422T>A , CM000676.2:g.24240422T>A	GRCh38
NC_000014.8:g.24709628T>A , CM000676.1:g.24709628T>A	GRCh37
NC_000014.7:g.23779468T>A	NCBI36
NG_016650.1:g.7253A>T
NG_054634.1:g.13006T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1361A>T
ENST00000557921.3:c.950A>T	ENSP00000453157.3:p.Lys317Met
ENST00000699682.1:n.1448A>T
ENST00000699683.1:n.1498A>T
ENST00000699684.1:c.*651A>T	ENSP00000514523.1:n.*651A>T
ENST00000699685.1:n.1262A>T
ENST00000699686.1:c.851A>T	ENSP00000514524.1:p.Lys284Met
ENST00000699687.1:c.953A>T	ENSP00000514525.1:p.Lys318Met
ENST00000699688.1:n.1258A>T
ENST00000699689.1:n.1614A>T
ENST00000699690.1:n.1811A>T
ENST00000699691.1:n.1955A>T
ENST00000699693.1:n.1475A>T
ENST00000699694.1:n.1717A>T
ENST00000699695.1:c.*430A>T	ENSP00000514526.1:n.*430A>T
ENST00000699696.1:n.1361A>T
ENST00000699697.1:c.1058A>T	ENSP00000514527.1:p.Lys353Met
ENST00000699698.1:n.979A>T
ENST00000699699.1:n.1382A>T
ENST00000699700.1:n.1505A>T
ENST00000699701.1:c.*438A>T	ENSP00000514528.1:n.*438A>T
ENST00000267415.12:c.1058A>T MANE Select	ENSP00000267415.7:p.Lys353Met
ENST00000646753.1:c.953A>T	ENSP00000494065.1:p.Lys318Met
ENST00000267415.11:c.1058A>T	ENSP00000267415.7:p.Lys353Met
ENST00000399423.8:c.1058A>T	ENSP00000382350.4:p.Lys353Met
ENST00000557915.1:n.177A>T
ENST00000558566.1:c.*430A>T	ENSP00000453025.1:n.*430A>T
ENST00000559969.5:c.816A>T
ENST00000560019.5:c.53A>T	ENSP00000453113.1:p.Lys18Met
ENST00000626689.2:c.*430A>T	ENSP00000486681.1:n.*430A>T
NM_001099274.1:c.1058A>T	NP_001092744.1:p.Lys353Met
NM_012461.2:c.1058A>T	NP_036593.2:p.Lys353Met
XM_005267528.2:c.1058A>T	XP_005267585.1:p.Lys353Met
XM_005267529.2:c.953A>T	XP_005267586.1:p.Lys318Met
NM_001099274.2:c.1058A>T	NP_001092744.1:p.Lys353Met
NM_001363668.1:c.953A>T	NP_001350597.1:p.Lys318Met
NM_012461.3:c.1058A>T	NP_036593.2:p.Lys353Met
XM_011536642.2:c.*438A>T	XP_011534944.1:n.*438A>T
XM_017021216.2:c.416A>T	XP_016876705.1:p.Lys139Met
XM_017021217.1:c.416A>T	XP_016876706.1:p.Lys139Met
NM_001099274.3:c.1058A>T MANE Select	NP_001092744.1:p.Lys353Met
NM_001363668.2:c.953A>T	NP_001350597.1:p.Lys318Met