Canonical Allele Identifier: CA389225386

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709823A>T (hg19) ; chr14:g.24240617A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240617A>T , CM000676.2:g.24240617A>T	GRCh38
NC_000014.8:g.24709823A>T , CM000676.1:g.24709823A>T	GRCh37
NC_000014.7:g.23779663A>T	NCBI36
NG_016650.1:g.7058T>A
NG_054634.1:g.13201A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1166T>A
ENST00000557921.3:c.755T>A	ENSP00000453157.3:p.Phe252Tyr
ENST00000699682.1:n.1253T>A
ENST00000699683.1:n.1303T>A
ENST00000699684.1:c.*456T>A	ENSP00000514523.1:n.*456T>A
ENST00000699685.1:n.1067T>A
ENST00000699686.1:c.656T>A	ENSP00000514524.1:p.Phe219Tyr
ENST00000699687.1:c.758T>A	ENSP00000514525.1:p.Phe253Tyr
ENST00000699688.1:n.1063T>A
ENST00000699689.1:n.1419T>A
ENST00000699690.1:n.1616T>A
ENST00000699691.1:n.1760T>A
ENST00000699693.1:n.1280T>A
ENST00000699694.1:n.1522T>A
ENST00000699695.1:c.*235T>A	ENSP00000514526.1:n.*235T>A
ENST00000699696.1:n.1166T>A
ENST00000699697.1:c.863T>A	ENSP00000514527.1:p.Phe288Tyr
ENST00000699698.1:n.784T>A
ENST00000699699.1:n.1187T>A
ENST00000699700.1:n.1310T>A
ENST00000699701.1:c.*243T>A	ENSP00000514528.1:n.*243T>A
ENST00000267415.12:c.863T>A MANE Select	ENSP00000267415.7:p.Phe288Tyr
ENST00000557921.2:c.755T>A	ENSP00000453157.2:p.Phe252Tyr
ENST00000646753.1:c.758T>A	ENSP00000494065.1:p.Phe253Tyr
ENST00000267415.11:c.863T>A	ENSP00000267415.7:p.Phe288Tyr
ENST00000399423.8:c.863T>A	ENSP00000382350.4:p.Phe288Tyr
ENST00000558476.5:c.425T>A	ENSP00000452724.1:p.Phe142Tyr
ENST00000558566.1:c.*235T>A	ENSP00000453025.1:n.*235T>A
ENST00000559019.1:c.*235T>A	ENSP00000453675.1:n.*235T>A
ENST00000559549.1:n.589T>A
ENST00000559969.5:c.757+62T>A
ENST00000626689.2:c.*235T>A	ENSP00000486681.1:n.*235T>A
NM_001099274.1:c.863T>A	NP_001092744.1:p.Phe288Tyr
NM_012461.2:c.863T>A	NP_036593.2:p.Phe288Tyr
XM_005267528.2:c.863T>A	XP_005267585.1:p.Phe288Tyr
XM_005267529.2:c.758T>A	XP_005267586.1:p.Phe253Tyr
NM_001099274.2:c.863T>A	NP_001092744.1:p.Phe288Tyr
NM_001363668.1:c.758T>A	NP_001350597.1:p.Phe253Tyr
NM_012461.3:c.863T>A	NP_036593.2:p.Phe288Tyr
XM_011536642.2:c.*243T>A	XP_011534944.1:n.*243T>A
XM_017021216.2:c.221T>A	XP_016876705.1:p.Phe74Tyr
XM_017021217.1:c.221T>A	XP_016876706.1:p.Phe74Tyr
NM_001099274.3:c.863T>A MANE Select	NP_001092744.1:p.Phe288Tyr
NM_001363668.2:c.758T>A	NP_001350597.1:p.Phe253Tyr