Canonical Allele Identifier: CA389223446

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709640G>T (hg19) ; chr14:g.24240434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240434G>T , CM000676.2:g.24240434G>T	GRCh38
NC_000014.8:g.24709640G>T , CM000676.1:g.24709640G>T	GRCh37
NC_000014.7:g.23779480G>T	NCBI36
NG_016650.1:g.7241C>A
NG_054634.1:g.13018G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1349C>A
ENST00000557921.3:c.938C>A	ENSP00000453157.3:p.Ala313Asp
ENST00000699682.1:n.1436C>A
ENST00000699683.1:n.1486C>A
ENST00000699684.1:c.*639C>A	ENSP00000514523.1:n.*639C>A
ENST00000699685.1:n.1250C>A
ENST00000699686.1:c.839C>A	ENSP00000514524.1:p.Ala280Asp
ENST00000699687.1:c.941C>A	ENSP00000514525.1:p.Ala314Asp
ENST00000699688.1:n.1246C>A
ENST00000699689.1:n.1602C>A
ENST00000699690.1:n.1799C>A
ENST00000699691.1:n.1943C>A
ENST00000699693.1:n.1463C>A
ENST00000699694.1:n.1705C>A
ENST00000699695.1:c.*418C>A	ENSP00000514526.1:n.*418C>A
ENST00000699696.1:n.1349C>A
ENST00000699697.1:c.1046C>A	ENSP00000514527.1:p.Ala349Asp
ENST00000699698.1:n.967C>A
ENST00000699699.1:n.1370C>A
ENST00000699700.1:n.1493C>A
ENST00000699701.1:c.*426C>A	ENSP00000514528.1:n.*426C>A
ENST00000267415.12:c.1046C>A MANE Select	ENSP00000267415.7:p.Ala349Asp
ENST00000646753.1:c.941C>A	ENSP00000494065.1:p.Ala314Asp
ENST00000267415.11:c.1046C>A	ENSP00000267415.7:p.Ala349Asp
ENST00000399423.8:c.1046C>A	ENSP00000382350.4:p.Ala349Asp
ENST00000557915.1:n.165C>A
ENST00000558566.1:c.*418C>A	ENSP00000453025.1:n.*418C>A
ENST00000559969.5:c.804C>A
ENST00000560019.5:c.41C>A	ENSP00000453113.1:p.Ala14Asp
ENST00000626689.2:c.*418C>A	ENSP00000486681.1:n.*418C>A
NM_001099274.1:c.1046C>A	NP_001092744.1:p.Ala349Asp
NM_012461.2:c.1046C>A	NP_036593.2:p.Ala349Asp
XM_005267528.2:c.1046C>A	XP_005267585.1:p.Ala349Asp
XM_005267529.2:c.941C>A	XP_005267586.1:p.Ala314Asp
NM_001099274.2:c.1046C>A	NP_001092744.1:p.Ala349Asp
NM_001363668.1:c.941C>A	NP_001350597.1:p.Ala314Asp
NM_012461.3:c.1046C>A	NP_036593.2:p.Ala349Asp
XM_011536642.2:c.*426C>A	XP_011534944.1:n.*426C>A
XM_017021216.2:c.404C>A	XP_016876705.1:p.Ala135Asp
XM_017021217.1:c.404C>A	XP_016876706.1:p.Ala135Asp
NM_001099274.3:c.1046C>A MANE Select	NP_001092744.1:p.Ala349Asp
NM_001363668.2:c.941C>A	NP_001350597.1:p.Ala314Asp