Canonical Allele Identifier: CA389224174

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709724C>A (hg19) ; chr14:g.24240518C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240518C>A , CM000676.2:g.24240518C>A	GRCh38
NC_000014.8:g.24709724C>A , CM000676.1:g.24709724C>A	GRCh37
NC_000014.7:g.23779564C>A	NCBI36
NG_016650.1:g.7157G>T
NG_054634.1:g.13102C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1265G>T
ENST00000557921.3:c.854G>T	ENSP00000453157.3:p.Arg285Ile
ENST00000699682.1:n.1352G>T
ENST00000699683.1:n.1402G>T
ENST00000699684.1:c.*555G>T	ENSP00000514523.1:n.*555G>T
ENST00000699685.1:n.1166G>T
ENST00000699686.1:c.755G>T	ENSP00000514524.1:p.Arg252Ile
ENST00000699687.1:c.857G>T	ENSP00000514525.1:p.Arg286Ile
ENST00000699688.1:n.1162G>T
ENST00000699689.1:n.1518G>T
ENST00000699690.1:n.1715G>T
ENST00000699691.1:n.1859G>T
ENST00000699693.1:n.1379G>T
ENST00000699694.1:n.1621G>T
ENST00000699695.1:c.*334G>T	ENSP00000514526.1:n.*334G>T
ENST00000699696.1:n.1265G>T
ENST00000699697.1:c.962G>T	ENSP00000514527.1:p.Arg321Ile
ENST00000699698.1:n.883G>T
ENST00000699699.1:n.1286G>T
ENST00000699700.1:n.1409G>T
ENST00000699701.1:c.*342G>T	ENSP00000514528.1:n.*342G>T
ENST00000267415.12:c.962G>T MANE Select	ENSP00000267415.7:p.Arg321Ile
ENST00000557921.2:c.854G>T	ENSP00000453157.2:p.Arg285Ile
ENST00000646753.1:c.857G>T	ENSP00000494065.1:p.Arg286Ile
ENST00000267415.11:c.962G>T	ENSP00000267415.7:p.Arg321Ile
ENST00000399423.8:c.962G>T	ENSP00000382350.4:p.Arg321Ile
ENST00000557915.1:n.81G>T
ENST00000558566.1:c.*334G>T	ENSP00000453025.1:n.*334G>T
ENST00000559019.1:c.*334G>T	ENSP00000453675.1:n.*334G>T
ENST00000559969.5:c.758-38G>T
ENST00000626689.2:c.*334G>T	ENSP00000486681.1:n.*334G>T
NM_001099274.1:c.962G>T	NP_001092744.1:p.Arg321Ile
NM_012461.2:c.962G>T	NP_036593.2:p.Arg321Ile
XM_005267528.2:c.962G>T	XP_005267585.1:p.Arg321Ile
XM_005267529.2:c.857G>T	XP_005267586.1:p.Arg286Ile
NM_001099274.2:c.962G>T	NP_001092744.1:p.Arg321Ile
NM_001363668.1:c.857G>T	NP_001350597.1:p.Arg286Ile
NM_012461.3:c.962G>T	NP_036593.2:p.Arg321Ile
XM_011536642.2:c.*342G>T	XP_011534944.1:n.*342G>T
XM_017021216.2:c.320G>T	XP_016876705.1:p.Arg107Ile
XM_017021217.1:c.320G>T	XP_016876706.1:p.Arg107Ile
NM_001099274.3:c.962G>T MANE Select	NP_001092744.1:p.Arg321Ile
NM_001363668.2:c.857G>T	NP_001350597.1:p.Arg286Ile