Canonical Allele Identifier: CA389226143

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709883A>G (hg19) ; chr14:g.24240677A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240677A>G , CM000676.2:g.24240677A>G	GRCh38
NC_000014.8:g.24709883A>G , CM000676.1:g.24709883A>G	GRCh37
NC_000014.7:g.23779723A>G	NCBI36
NG_016650.1:g.6998T>C
NG_054634.1:g.13261A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1106T>C
ENST00000557921.3:c.695T>C	ENSP00000453157.3:p.Val232Ala
ENST00000699682.1:n.1193T>C
ENST00000699683.1:n.1243T>C
ENST00000699684.1:c.*396T>C	ENSP00000514523.1:n.*396T>C
ENST00000699685.1:n.1007T>C
ENST00000699686.1:c.596T>C	ENSP00000514524.1:p.Val199Ala
ENST00000699687.1:c.698T>C	ENSP00000514525.1:p.Val233Ala
ENST00000699688.1:n.1003T>C
ENST00000699689.1:n.1359T>C
ENST00000699690.1:n.1556T>C
ENST00000699691.1:n.1700T>C
ENST00000699693.1:n.1220T>C
ENST00000699694.1:n.1462T>C
ENST00000699695.1:c.*175T>C	ENSP00000514526.1:n.*175T>C
ENST00000699696.1:n.1106T>C
ENST00000699697.1:c.803T>C	ENSP00000514527.1:p.Val268Ala
ENST00000699698.1:n.724T>C
ENST00000699699.1:n.1127T>C
ENST00000699700.1:n.1250T>C
ENST00000699701.1:c.*183T>C	ENSP00000514528.1:n.*183T>C
ENST00000267415.12:c.803T>C MANE Select	ENSP00000267415.7:p.Val268Ala
ENST00000557921.2:c.695T>C	ENSP00000453157.2:p.Val232Ala
ENST00000646753.1:c.698T>C	ENSP00000494065.1:p.Val233Ala
ENST00000267415.11:c.803T>C	ENSP00000267415.7:p.Val268Ala
ENST00000399423.8:c.803T>C	ENSP00000382350.4:p.Val268Ala
ENST00000558476.5:c.365T>C	ENSP00000452724.1:p.Val122Ala
ENST00000558566.1:c.*175T>C	ENSP00000453025.1:n.*175T>C
ENST00000559019.1:c.*175T>C	ENSP00000453675.1:n.*175T>C
ENST00000559549.1:n.529T>C
ENST00000559969.5:c.757+2T>C
ENST00000626689.2:c.*175T>C	ENSP00000486681.1:n.*175T>C
NM_001099274.1:c.803T>C	NP_001092744.1:p.Val268Ala
NM_012461.2:c.803T>C	NP_036593.2:p.Val268Ala
XM_005267528.2:c.803T>C	XP_005267585.1:p.Val268Ala
XM_005267529.2:c.698T>C	XP_005267586.1:p.Val233Ala
NM_001099274.2:c.803T>C	NP_001092744.1:p.Val268Ala
NM_001363668.1:c.698T>C	NP_001350597.1:p.Val233Ala
NM_012461.3:c.803T>C	NP_036593.2:p.Val268Ala
XM_011536642.2:c.*183T>C	XP_011534944.1:n.*183T>C
XM_017021216.2:c.161T>C	XP_016876705.1:p.Val54Ala
XM_017021217.1:c.161T>C	XP_016876706.1:p.Val54Ala
NM_001099274.3:c.803T>C MANE Select	NP_001092744.1:p.Val268Ala
NM_001363668.2:c.698T>C	NP_001350597.1:p.Val233Ala