Canonical Allele Identifier: CA485782149

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709639G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240433G>C , CM000676.2:g.24240433G>C	GRCh38
NC_000014.8:g.24709639G>C , CM000676.1:g.24709639G>C	GRCh37
NC_000014.7:g.23779479G>C	NCBI36
NG_016650.1:g.7242C>G
NG_054634.1:g.13017G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1350C>G
ENST00000557921.3:c.939C>G	ENSP00000453157.3:p.Ala313=
ENST00000699682.1:n.1437C>G
ENST00000699683.1:n.1487C>G
ENST00000699684.1:c.*640C>G	ENSP00000514523.1:n.*640C>G
ENST00000699685.1:n.1251C>G
ENST00000699686.1:c.840C>G	ENSP00000514524.1:p.Ala280=
ENST00000699687.1:c.942C>G	ENSP00000514525.1:p.Ala314=
ENST00000699688.1:n.1247C>G
ENST00000699689.1:n.1603C>G
ENST00000699690.1:n.1800C>G
ENST00000699691.1:n.1944C>G
ENST00000699693.1:n.1464C>G
ENST00000699694.1:n.1706C>G
ENST00000699695.1:c.*419C>G	ENSP00000514526.1:n.*419C>G
ENST00000699696.1:n.1350C>G
ENST00000699697.1:c.1047C>G	ENSP00000514527.1:p.Ala349=
ENST00000699698.1:n.968C>G
ENST00000699699.1:n.1371C>G
ENST00000699700.1:n.1494C>G
ENST00000699701.1:c.*427C>G	ENSP00000514528.1:n.*427C>G
ENST00000267415.12:c.1047C>G MANE Select	ENSP00000267415.7:p.Ala349=
ENST00000646753.1:c.942C>G	ENSP00000494065.1:p.Ala314=
ENST00000267415.11:c.1047C>G	ENSP00000267415.7:p.Ala349=
ENST00000399423.8:c.1047C>G	ENSP00000382350.4:p.Ala349=
ENST00000557915.1:n.166C>G
ENST00000558566.1:c.*419C>G	ENSP00000453025.1:n.*419C>G
ENST00000559969.5:c.805C>G
ENST00000560019.5:c.42C>G	ENSP00000453113.1:p.Ala14=
ENST00000626689.2:c.*419C>G	ENSP00000486681.1:n.*419C>G
NM_001099274.1:c.1047C>G	NP_001092744.1:p.Ala349=
NM_012461.2:c.1047C>G	NP_036593.2:p.Ala349=
XM_005267528.2:c.1047C>G	XP_005267585.1:p.Ala349=
XM_005267529.2:c.942C>G	XP_005267586.1:p.Ala314=
NM_001099274.2:c.1047C>G	NP_001092744.1:p.Ala349=
NM_001363668.1:c.942C>G	NP_001350597.1:p.Ala314=
NM_012461.3:c.1047C>G	NP_036593.2:p.Ala349=
XM_011536642.2:c.*427C>G	XP_011534944.1:n.*427C>G
XM_017021216.2:c.405C>G	XP_016876705.1:p.Ala135=
XM_017021217.1:c.405C>G	XP_016876706.1:p.Ala135=
NM_001099274.3:c.1047C>G MANE Select	NP_001092744.1:p.Ala349=
NM_001363668.2:c.942C>G	NP_001350597.1:p.Ala314=