Canonical Allele Identifier: CA389226487

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709914A>C (hg19) ; chr14:g.24240708A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240708A>C , CM000676.2:g.24240708A>C	GRCh38
NC_000014.8:g.24709914A>C , CM000676.1:g.24709914A>C	GRCh37
NC_000014.7:g.23779754A>C	NCBI36
NG_016650.1:g.6967T>G
NG_054634.1:g.13292A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1075T>G
ENST00000557921.3:c.664T>G	ENSP00000453157.3:p.Phe222Val
ENST00000699682.1:n.1162T>G
ENST00000699683.1:n.1212T>G
ENST00000699684.1:c.*365T>G	ENSP00000514523.1:n.*365T>G
ENST00000699685.1:n.976T>G
ENST00000699686.1:c.565T>G	ENSP00000514524.1:p.Phe189Val
ENST00000699687.1:c.667T>G	ENSP00000514525.1:p.Phe223Val
ENST00000699688.1:n.972T>G
ENST00000699689.1:n.1328T>G
ENST00000699690.1:n.1525T>G
ENST00000699691.1:n.1669T>G
ENST00000699693.1:n.1189T>G
ENST00000699694.1:n.1431T>G
ENST00000699695.1:c.*144T>G	ENSP00000514526.1:n.*144T>G
ENST00000699696.1:n.1075T>G
ENST00000699697.1:c.772T>G	ENSP00000514527.1:p.Phe258Val
ENST00000699698.1:n.693T>G
ENST00000699699.1:n.1096T>G
ENST00000699700.1:n.1219T>G
ENST00000699701.1:c.*152T>G	ENSP00000514528.1:n.*152T>G
ENST00000267415.12:c.772T>G MANE Select	ENSP00000267415.7:p.Phe258Val
ENST00000557921.2:c.664T>G	ENSP00000453157.2:p.Phe222Val
ENST00000646753.1:c.667T>G	ENSP00000494065.1:p.Phe223Val
ENST00000267415.11:c.772T>G	ENSP00000267415.7:p.Phe258Val
ENST00000399423.8:c.772T>G	ENSP00000382350.4:p.Phe258Val
ENST00000558476.5:c.334T>G	ENSP00000452724.1:p.Phe112Val
ENST00000558566.1:c.*144T>G	ENSP00000453025.1:n.*144T>G
ENST00000559019.1:c.*144T>G	ENSP00000453675.1:n.*144T>G
ENST00000559549.1:n.498T>G
ENST00000559969.5:c.728T>G
ENST00000626689.2:c.*144T>G	ENSP00000486681.1:n.*144T>G
NM_001099274.1:c.772T>G	NP_001092744.1:p.Phe258Val
NM_012461.2:c.772T>G	NP_036593.2:p.Phe258Val
XM_005267528.2:c.772T>G	XP_005267585.1:p.Phe258Val
XM_005267529.2:c.667T>G	XP_005267586.1:p.Phe223Val
NM_001099274.2:c.772T>G	NP_001092744.1:p.Phe258Val
NM_001363668.1:c.667T>G	NP_001350597.1:p.Phe223Val
NM_012461.3:c.772T>G	NP_036593.2:p.Phe258Val
XM_011536642.2:c.*152T>G	XP_011534944.1:n.*152T>G
XM_017021216.2:c.130T>G	XP_016876705.1:p.Phe44Val
XM_017021217.1:c.130T>G	XP_016876706.1:p.Phe44Val
NM_001099274.3:c.772T>G MANE Select	NP_001092744.1:p.Phe258Val
NM_001363668.2:c.667T>G	NP_001350597.1:p.Phe223Val