Canonical Allele Identifier: CA485782275

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709924A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240718A>T , CM000676.2:g.24240718A>T	GRCh38
NC_000014.8:g.24709924A>T , CM000676.1:g.24709924A>T	GRCh37
NC_000014.7:g.23779764A>T	NCBI36
NG_016650.1:g.6957T>A
NG_054634.1:g.13302A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1065T>A
ENST00000557921.3:c.654T>A	ENSP00000453157.3:p.Ala218=
ENST00000699682.1:n.1152T>A
ENST00000699683.1:n.1202T>A
ENST00000699684.1:c.*355T>A	ENSP00000514523.1:n.*355T>A
ENST00000699685.1:n.966T>A
ENST00000699686.1:c.555T>A	ENSP00000514524.1:p.Ala185=
ENST00000699687.1:c.657T>A	ENSP00000514525.1:p.Ala219=
ENST00000699688.1:n.962T>A
ENST00000699689.1:n.1318T>A
ENST00000699690.1:n.1515T>A
ENST00000699691.1:n.1659T>A
ENST00000699693.1:n.1179T>A
ENST00000699694.1:n.1421T>A
ENST00000699695.1:c.*134T>A	ENSP00000514526.1:n.*134T>A
ENST00000699696.1:n.1065T>A
ENST00000699697.1:c.762T>A	ENSP00000514527.1:p.Ala254=
ENST00000699698.1:n.683T>A
ENST00000699699.1:n.1086T>A
ENST00000699700.1:n.1209T>A
ENST00000699701.1:c.*142T>A	ENSP00000514528.1:n.*142T>A
ENST00000267415.12:c.762T>A MANE Select	ENSP00000267415.7:p.Ala254=
ENST00000557921.2:c.654T>A	ENSP00000453157.2:p.Ala218=
ENST00000646753.1:c.657T>A	ENSP00000494065.1:p.Ala219=
ENST00000267415.11:c.762T>A	ENSP00000267415.7:p.Ala254=
ENST00000399423.8:c.762T>A	ENSP00000382350.4:p.Ala254=
ENST00000558476.5:c.324T>A	ENSP00000452724.1:p.Ala108=
ENST00000558566.1:c.*134T>A	ENSP00000453025.1:n.*134T>A
ENST00000559019.1:c.*134T>A	ENSP00000453675.1:n.*134T>A
ENST00000559549.1:n.488T>A
ENST00000559969.5:c.718T>A
ENST00000626689.2:c.*134T>A	ENSP00000486681.1:n.*134T>A
NM_001099274.1:c.762T>A	NP_001092744.1:p.Ala254=
NM_012461.2:c.762T>A	NP_036593.2:p.Ala254=
XM_005267528.2:c.762T>A	XP_005267585.1:p.Ala254=
XM_005267529.2:c.657T>A	XP_005267586.1:p.Ala219=
NM_001099274.2:c.762T>A	NP_001092744.1:p.Ala254=
NM_001363668.1:c.657T>A	NP_001350597.1:p.Ala219=
NM_012461.3:c.762T>A	NP_036593.2:p.Ala254=
XM_011536642.2:c.*142T>A	XP_011534944.1:n.*142T>A
XM_017021216.2:c.120T>A	XP_016876705.1:p.Ala40=
XM_017021217.1:c.120T>A	XP_016876706.1:p.Ala40=
NM_001099274.3:c.762T>A MANE Select	NP_001092744.1:p.Ala254=
NM_001363668.2:c.657T>A	NP_001350597.1:p.Ala219=