Canonical Allele Identifier: CA485782032

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709500T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240294T>C , CM000676.2:g.24240294T>C	GRCh38
NC_000014.8:g.24709500T>C , CM000676.1:g.24709500T>C	GRCh37
NC_000014.7:g.23779340T>C	NCBI36
NG_016650.1:g.7381A>G
NG_054634.1:g.12878T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1489A>G
ENST00000557921.3:c.*121A>G	ENSP00000453157.3:n.*121A>G
ENST00000699682.1:n.1576A>G
ENST00000699683.1:n.1626A>G
ENST00000699684.1:c.*779A>G	ENSP00000514523.1:n.*779A>G
ENST00000699685.1:n.1390A>G
ENST00000699686.1:c.*121A>G	ENSP00000514524.1:n.*121A>G
ENST00000699687.1:c.*121A>G	ENSP00000514525.1:n.*121A>G
ENST00000699688.1:n.1386A>G
ENST00000699689.1:n.1742A>G
ENST00000699690.1:n.1939A>G
ENST00000699691.1:n.2083A>G
ENST00000699692.1:n.37A>G
ENST00000699693.1:n.1515A>G
ENST00000699694.1:n.1845A>G
ENST00000699695.1:c.*470A>G	ENSP00000514526.1:n.*470A>G
ENST00000699696.1:n.1489A>G
ENST00000699697.1:c.1098A>G	ENSP00000514527.1:p.Leu366=
ENST00000699698.1:n.1019A>G
ENST00000699699.1:n.1510A>G
ENST00000699700.1:n.1633A>G
ENST00000699701.1:c.*566A>G	ENSP00000514528.1:n.*566A>G
ENST00000267415.12:c.1098A>G MANE Select	ENSP00000267415.7:p.Leu366=
ENST00000646753.1:c.993A>G	ENSP00000494065.1:p.Leu331=
ENST00000267415.11:c.1098A>G	ENSP00000267415.7:p.Leu366=
ENST00000399423.8:c.*121A>G	ENSP00000382350.4:n.*121A>G
ENST00000557915.1:n.305A>G
ENST00000558566.1:c.*558A>G	ENSP00000453025.1:n.*558A>G
ENST00000559969.5:c.944A>G
ENST00000560019.5:c.93A>G	ENSP00000453113.1:p.Leu31=
ENST00000626689.2:c.*470A>G	ENSP00000486681.1:n.*470A>G
NM_001099274.1:c.1098A>G	NP_001092744.1:p.Leu366=
NM_012461.2:c.*121A>G	NP_036593.2:n.*121A>G
XM_005267528.2:c.1098A>G	XP_005267585.1:p.Leu366=
XM_005267529.2:c.993A>G	XP_005267586.1:p.Leu331=
NM_001099274.2:c.1098A>G	NP_001092744.1:p.Leu366=
NM_001363668.1:c.993A>G	NP_001350597.1:p.Leu331=
NM_012461.3:c.*121A>G	NP_036593.2:n.*121A>G
XM_011536642.2:c.*566A>G	XP_011534944.1:n.*566A>G
XM_017021216.2:c.456A>G	XP_016876705.1:p.Leu152=
XM_017021217.1:c.456A>G	XP_016876706.1:p.Leu152=
NM_001099274.3:c.1098A>G MANE Select	NP_001092744.1:p.Leu366=
NM_001363668.2:c.993A>G	NP_001350597.1:p.Leu331=