Canonical Allele Identifier: CA389226613

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709926C>A (hg19) ; chr14:g.24240720C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240720C>A , CM000676.2:g.24240720C>A	GRCh38
NC_000014.8:g.24709926C>A , CM000676.1:g.24709926C>A	GRCh37
NC_000014.7:g.23779766C>A	NCBI36
NG_016650.1:g.6955G>T
NG_054634.1:g.13304C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1063G>T
ENST00000557921.3:c.652G>T	ENSP00000453157.3:p.Ala218Ser
ENST00000699682.1:n.1150G>T
ENST00000699683.1:n.1200G>T
ENST00000699684.1:c.*353G>T	ENSP00000514523.1:n.*353G>T
ENST00000699685.1:n.964G>T
ENST00000699686.1:c.553G>T	ENSP00000514524.1:p.Ala185Ser
ENST00000699687.1:c.655G>T	ENSP00000514525.1:p.Ala219Ser
ENST00000699688.1:n.960G>T
ENST00000699689.1:n.1316G>T
ENST00000699690.1:n.1513G>T
ENST00000699691.1:n.1657G>T
ENST00000699693.1:n.1177G>T
ENST00000699694.1:n.1419G>T
ENST00000699695.1:c.*132G>T	ENSP00000514526.1:n.*132G>T
ENST00000699696.1:n.1063G>T
ENST00000699697.1:c.760G>T	ENSP00000514527.1:p.Ala254Ser
ENST00000699698.1:n.681G>T
ENST00000699699.1:n.1084G>T
ENST00000699700.1:n.1207G>T
ENST00000699701.1:c.*140G>T	ENSP00000514528.1:n.*140G>T
ENST00000267415.12:c.760G>T MANE Select	ENSP00000267415.7:p.Ala254Ser
ENST00000557921.2:c.652G>T	ENSP00000453157.2:p.Ala218Ser
ENST00000646753.1:c.655G>T	ENSP00000494065.1:p.Ala219Ser
ENST00000267415.11:c.760G>T	ENSP00000267415.7:p.Ala254Ser
ENST00000399423.8:c.760G>T	ENSP00000382350.4:p.Ala254Ser
ENST00000558476.5:c.322G>T	ENSP00000452724.1:p.Ala108Ser
ENST00000558566.1:c.*132G>T	ENSP00000453025.1:n.*132G>T
ENST00000559019.1:c.*132G>T	ENSP00000453675.1:n.*132G>T
ENST00000559549.1:n.486G>T
ENST00000559969.5:c.716G>T
ENST00000626689.2:c.*132G>T	ENSP00000486681.1:n.*132G>T
NM_001099274.1:c.760G>T	NP_001092744.1:p.Ala254Ser
NM_012461.2:c.760G>T	NP_036593.2:p.Ala254Ser
XM_005267528.2:c.760G>T	XP_005267585.1:p.Ala254Ser
XM_005267529.2:c.655G>T	XP_005267586.1:p.Ala219Ser
NM_001099274.2:c.760G>T	NP_001092744.1:p.Ala254Ser
NM_001363668.1:c.655G>T	NP_001350597.1:p.Ala219Ser
NM_012461.3:c.760G>T	NP_036593.2:p.Ala254Ser
XM_011536642.2:c.*140G>T	XP_011534944.1:n.*140G>T
XM_017021216.2:c.118G>T	XP_016876705.1:p.Ala40Ser
XM_017021217.1:c.118G>T	XP_016876706.1:p.Ala40Ser
NM_001099274.3:c.760G>T MANE Select	NP_001092744.1:p.Ala254Ser
NM_001363668.2:c.655G>T	NP_001350597.1:p.Ala219Ser