Canonical Allele Identifier: CA389224233

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709728T>A (hg19) ; chr14:g.24240522T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240522T>A , CM000676.2:g.24240522T>A	GRCh38
NC_000014.8:g.24709728T>A , CM000676.1:g.24709728T>A	GRCh37
NC_000014.7:g.23779568T>A	NCBI36
NG_016650.1:g.7153A>T
NG_054634.1:g.13106T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1261A>T
ENST00000557921.3:c.850A>T	ENSP00000453157.3:p.Thr284Ser
ENST00000699682.1:n.1348A>T
ENST00000699683.1:n.1398A>T
ENST00000699684.1:c.*551A>T	ENSP00000514523.1:n.*551A>T
ENST00000699685.1:n.1162A>T
ENST00000699686.1:c.751A>T	ENSP00000514524.1:p.Thr251Ser
ENST00000699687.1:c.853A>T	ENSP00000514525.1:p.Thr285Ser
ENST00000699688.1:n.1158A>T
ENST00000699689.1:n.1514A>T
ENST00000699690.1:n.1711A>T
ENST00000699691.1:n.1855A>T
ENST00000699693.1:n.1375A>T
ENST00000699694.1:n.1617A>T
ENST00000699695.1:c.*330A>T	ENSP00000514526.1:n.*330A>T
ENST00000699696.1:n.1261A>T
ENST00000699697.1:c.958A>T	ENSP00000514527.1:p.Thr320Ser
ENST00000699698.1:n.879A>T
ENST00000699699.1:n.1282A>T
ENST00000699700.1:n.1405A>T
ENST00000699701.1:c.*338A>T	ENSP00000514528.1:n.*338A>T
ENST00000267415.12:c.958A>T MANE Select	ENSP00000267415.7:p.Thr320Ser
ENST00000557921.2:c.850A>T	ENSP00000453157.2:p.Thr284Ser
ENST00000646753.1:c.853A>T	ENSP00000494065.1:p.Thr285Ser
ENST00000267415.11:c.958A>T	ENSP00000267415.7:p.Thr320Ser
ENST00000399423.8:c.958A>T	ENSP00000382350.4:p.Thr320Ser
ENST00000557915.1:n.77A>T
ENST00000558566.1:c.*330A>T	ENSP00000453025.1:n.*330A>T
ENST00000559019.1:c.*330A>T	ENSP00000453675.1:n.*330A>T
ENST00000559969.5:c.758-42A>T
ENST00000626689.2:c.*330A>T	ENSP00000486681.1:n.*330A>T
NM_001099274.1:c.958A>T	NP_001092744.1:p.Thr320Ser
NM_012461.2:c.958A>T	NP_036593.2:p.Thr320Ser
XM_005267528.2:c.958A>T	XP_005267585.1:p.Thr320Ser
XM_005267529.2:c.853A>T	XP_005267586.1:p.Thr285Ser
NM_001099274.2:c.958A>T	NP_001092744.1:p.Thr320Ser
NM_001363668.1:c.853A>T	NP_001350597.1:p.Thr285Ser
NM_012461.3:c.958A>T	NP_036593.2:p.Thr320Ser
XM_011536642.2:c.*338A>T	XP_011534944.1:n.*338A>T
XM_017021216.2:c.316A>T	XP_016876705.1:p.Thr106Ser
XM_017021217.1:c.316A>T	XP_016876706.1:p.Thr106Ser
NM_001099274.3:c.958A>T MANE Select	NP_001092744.1:p.Thr320Ser
NM_001363668.2:c.853A>T	NP_001350597.1:p.Thr285Ser