Canonical Allele Identifier: CA485782118

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709813C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240607C>T , CM000676.2:g.24240607C>T	GRCh38
NC_000014.8:g.24709813C>T , CM000676.1:g.24709813C>T	GRCh37
NC_000014.7:g.23779653C>T	NCBI36
NG_016650.1:g.7068G>A
NG_054634.1:g.13191C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1176G>A
ENST00000557921.3:c.765G>A	ENSP00000453157.3:p.Arg255=
ENST00000699682.1:n.1263G>A
ENST00000699683.1:n.1313G>A
ENST00000699684.1:c.*466G>A	ENSP00000514523.1:n.*466G>A
ENST00000699685.1:n.1077G>A
ENST00000699686.1:c.666G>A	ENSP00000514524.1:p.Arg222=
ENST00000699687.1:c.768G>A	ENSP00000514525.1:p.Arg256=
ENST00000699688.1:n.1073G>A
ENST00000699689.1:n.1429G>A
ENST00000699690.1:n.1626G>A
ENST00000699691.1:n.1770G>A
ENST00000699693.1:n.1290G>A
ENST00000699694.1:n.1532G>A
ENST00000699695.1:c.*245G>A	ENSP00000514526.1:n.*245G>A
ENST00000699696.1:n.1176G>A
ENST00000699697.1:c.873G>A	ENSP00000514527.1:p.Arg291=
ENST00000699698.1:n.794G>A
ENST00000699699.1:n.1197G>A
ENST00000699700.1:n.1320G>A
ENST00000699701.1:c.*253G>A	ENSP00000514528.1:n.*253G>A
ENST00000267415.12:c.873G>A MANE Select	ENSP00000267415.7:p.Arg291=
ENST00000557921.2:c.765G>A	ENSP00000453157.2:p.Arg255=
ENST00000646753.1:c.768G>A	ENSP00000494065.1:p.Arg256=
ENST00000267415.11:c.873G>A	ENSP00000267415.7:p.Arg291=
ENST00000399423.8:c.873G>A	ENSP00000382350.4:p.Arg291=
ENST00000558476.5:c.435G>A	ENSP00000452724.1:p.Arg145=
ENST00000558566.1:c.*245G>A	ENSP00000453025.1:n.*245G>A
ENST00000559019.1:c.*245G>A	ENSP00000453675.1:n.*245G>A
ENST00000559549.1:n.599G>A
ENST00000559969.5:c.757+72G>A
ENST00000626689.2:c.*245G>A	ENSP00000486681.1:n.*245G>A
NM_001099274.1:c.873G>A	NP_001092744.1:p.Arg291=
NM_012461.2:c.873G>A	NP_036593.2:p.Arg291=
XM_005267528.2:c.873G>A	XP_005267585.1:p.Arg291=
XM_005267529.2:c.768G>A	XP_005267586.1:p.Arg256=
NM_001099274.2:c.873G>A	NP_001092744.1:p.Arg291=
NM_001363668.1:c.768G>A	NP_001350597.1:p.Arg256=
NM_012461.3:c.873G>A	NP_036593.2:p.Arg291=
XM_011536642.2:c.*253G>A	XP_011534944.1:n.*253G>A
XM_017021216.2:c.231G>A	XP_016876705.1:p.Arg77=
XM_017021217.1:c.231G>A	XP_016876706.1:p.Arg77=
NM_001099274.3:c.873G>A MANE Select	NP_001092744.1:p.Arg291=
NM_001363668.2:c.768G>A	NP_001350597.1:p.Arg256=