Canonical Allele Identifier: CA485782219

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709894G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240688G>C , CM000676.2:g.24240688G>C	GRCh38
NC_000014.8:g.24709894G>C , CM000676.1:g.24709894G>C	GRCh37
NC_000014.7:g.23779734G>C	NCBI36
NG_016650.1:g.6987C>G
NG_054634.1:g.13272G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1095C>G
ENST00000557921.3:c.684C>G	ENSP00000453157.3:p.Gly228=
ENST00000699682.1:n.1182C>G
ENST00000699683.1:n.1232C>G
ENST00000699684.1:c.*385C>G	ENSP00000514523.1:n.*385C>G
ENST00000699685.1:n.996C>G
ENST00000699686.1:c.585C>G	ENSP00000514524.1:p.Gly195=
ENST00000699687.1:c.687C>G	ENSP00000514525.1:p.Gly229=
ENST00000699688.1:n.992C>G
ENST00000699689.1:n.1348C>G
ENST00000699690.1:n.1545C>G
ENST00000699691.1:n.1689C>G
ENST00000699693.1:n.1209C>G
ENST00000699694.1:n.1451C>G
ENST00000699695.1:c.*164C>G	ENSP00000514526.1:n.*164C>G
ENST00000699696.1:n.1095C>G
ENST00000699697.1:c.792C>G	ENSP00000514527.1:p.Gly264=
ENST00000699698.1:n.713C>G
ENST00000699699.1:n.1116C>G
ENST00000699700.1:n.1239C>G
ENST00000699701.1:c.*172C>G	ENSP00000514528.1:n.*172C>G
ENST00000267415.12:c.792C>G MANE Select	ENSP00000267415.7:p.Gly264=
ENST00000557921.2:c.684C>G	ENSP00000453157.2:p.Gly228=
ENST00000646753.1:c.687C>G	ENSP00000494065.1:p.Gly229=
ENST00000267415.11:c.792C>G	ENSP00000267415.7:p.Gly264=
ENST00000399423.8:c.792C>G	ENSP00000382350.4:p.Gly264=
ENST00000558476.5:c.354C>G	ENSP00000452724.1:p.Gly118=
ENST00000558566.1:c.*164C>G	ENSP00000453025.1:n.*164C>G
ENST00000559019.1:c.*164C>G	ENSP00000453675.1:n.*164C>G
ENST00000559549.1:n.518C>G
ENST00000559969.5:c.748C>G
ENST00000626689.2:c.*164C>G	ENSP00000486681.1:n.*164C>G
NM_001099274.1:c.792C>G	NP_001092744.1:p.Gly264=
NM_012461.2:c.792C>G	NP_036593.2:p.Gly264=
XM_005267528.2:c.792C>G	XP_005267585.1:p.Gly264=
XM_005267529.2:c.687C>G	XP_005267586.1:p.Gly229=
NM_001099274.2:c.792C>G	NP_001092744.1:p.Gly264=
NM_001363668.1:c.687C>G	NP_001350597.1:p.Gly229=
NM_012461.3:c.792C>G	NP_036593.2:p.Gly264=
XM_011536642.2:c.*172C>G	XP_011534944.1:n.*172C>G
XM_017021216.2:c.150C>G	XP_016876705.1:p.Gly50=
XM_017021217.1:c.150C>G	XP_016876706.1:p.Gly50=
NM_001099274.3:c.792C>G MANE Select	NP_001092744.1:p.Gly264=
NM_001363668.2:c.687C>G	NP_001350597.1:p.Gly229=