Canonical Allele Identifier: CA485782129

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709831G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240625G>C , CM000676.2:g.24240625G>C	GRCh38
NC_000014.8:g.24709831G>C , CM000676.1:g.24709831G>C	GRCh37
NC_000014.7:g.23779671G>C	NCBI36
NG_016650.1:g.7050C>G
NG_054634.1:g.13209G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1158C>G
ENST00000557921.3:c.747C>G	ENSP00000453157.3:p.Val249=
ENST00000699682.1:n.1245C>G
ENST00000699683.1:n.1295C>G
ENST00000699684.1:c.*448C>G	ENSP00000514523.1:n.*448C>G
ENST00000699685.1:n.1059C>G
ENST00000699686.1:c.648C>G	ENSP00000514524.1:p.Val216=
ENST00000699687.1:c.750C>G	ENSP00000514525.1:p.Val250=
ENST00000699688.1:n.1055C>G
ENST00000699689.1:n.1411C>G
ENST00000699690.1:n.1608C>G
ENST00000699691.1:n.1752C>G
ENST00000699693.1:n.1272C>G
ENST00000699694.1:n.1514C>G
ENST00000699695.1:c.*227C>G	ENSP00000514526.1:n.*227C>G
ENST00000699696.1:n.1158C>G
ENST00000699697.1:c.855C>G	ENSP00000514527.1:p.Val285=
ENST00000699698.1:n.776C>G
ENST00000699699.1:n.1179C>G
ENST00000699700.1:n.1302C>G
ENST00000699701.1:c.*235C>G	ENSP00000514528.1:n.*235C>G
ENST00000267415.12:c.855C>G MANE Select	ENSP00000267415.7:p.Val285=
ENST00000557921.2:c.747C>G	ENSP00000453157.2:p.Val249=
ENST00000646753.1:c.750C>G	ENSP00000494065.1:p.Val250=
ENST00000267415.11:c.855C>G	ENSP00000267415.7:p.Val285=
ENST00000399423.8:c.855C>G	ENSP00000382350.4:p.Val285=
ENST00000558476.5:c.417C>G	ENSP00000452724.1:p.Val139=
ENST00000558566.1:c.*227C>G	ENSP00000453025.1:n.*227C>G
ENST00000559019.1:c.*227C>G	ENSP00000453675.1:n.*227C>G
ENST00000559549.1:n.581C>G
ENST00000559969.5:c.757+54C>G
ENST00000626689.2:c.*227C>G	ENSP00000486681.1:n.*227C>G
NM_001099274.1:c.855C>G	NP_001092744.1:p.Val285=
NM_012461.2:c.855C>G	NP_036593.2:p.Val285=
XM_005267528.2:c.855C>G	XP_005267585.1:p.Val285=
XM_005267529.2:c.750C>G	XP_005267586.1:p.Val250=
NM_001099274.2:c.855C>G	NP_001092744.1:p.Val285=
NM_001363668.1:c.750C>G	NP_001350597.1:p.Val250=
NM_012461.3:c.855C>G	NP_036593.2:p.Val285=
XM_011536642.2:c.*235C>G	XP_011534944.1:n.*235C>G
XM_017021216.2:c.213C>G	XP_016876705.1:p.Val71=
XM_017021217.1:c.213C>G	XP_016876706.1:p.Val71=
NM_001099274.3:c.855C>G MANE Select	NP_001092744.1:p.Val285=
NM_001363668.2:c.750C>G	NP_001350597.1:p.Val250=