Canonical Allele Identifier: CA485782159

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709861A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240655A>C , CM000676.2:g.24240655A>C	GRCh38
NC_000014.8:g.24709861A>C , CM000676.1:g.24709861A>C	GRCh37
NC_000014.7:g.23779701A>C	NCBI36
NG_016650.1:g.7020T>G
NG_054634.1:g.13239A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1128T>G
ENST00000557921.3:c.717T>G	ENSP00000453157.3:p.Thr239=
ENST00000699682.1:n.1215T>G
ENST00000699683.1:n.1265T>G
ENST00000699684.1:c.*418T>G	ENSP00000514523.1:n.*418T>G
ENST00000699685.1:n.1029T>G
ENST00000699686.1:c.618T>G	ENSP00000514524.1:p.Thr206=
ENST00000699687.1:c.720T>G	ENSP00000514525.1:p.Thr240=
ENST00000699688.1:n.1025T>G
ENST00000699689.1:n.1381T>G
ENST00000699690.1:n.1578T>G
ENST00000699691.1:n.1722T>G
ENST00000699693.1:n.1242T>G
ENST00000699694.1:n.1484T>G
ENST00000699695.1:c.*197T>G	ENSP00000514526.1:n.*197T>G
ENST00000699696.1:n.1128T>G
ENST00000699697.1:c.825T>G	ENSP00000514527.1:p.Thr275=
ENST00000699698.1:n.746T>G
ENST00000699699.1:n.1149T>G
ENST00000699700.1:n.1272T>G
ENST00000699701.1:c.*205T>G	ENSP00000514528.1:n.*205T>G
ENST00000267415.12:c.825T>G MANE Select	ENSP00000267415.7:p.Thr275=
ENST00000557921.2:c.717T>G	ENSP00000453157.2:p.Thr239=
ENST00000646753.1:c.720T>G	ENSP00000494065.1:p.Thr240=
ENST00000267415.11:c.825T>G	ENSP00000267415.7:p.Thr275=
ENST00000399423.8:c.825T>G	ENSP00000382350.4:p.Thr275=
ENST00000558476.5:c.387T>G	ENSP00000452724.1:p.Thr129=
ENST00000558566.1:c.*197T>G	ENSP00000453025.1:n.*197T>G
ENST00000559019.1:c.*197T>G	ENSP00000453675.1:n.*197T>G
ENST00000559549.1:n.551T>G
ENST00000559969.5:c.757+24T>G
ENST00000626689.2:c.*197T>G	ENSP00000486681.1:n.*197T>G
NM_001099274.1:c.825T>G	NP_001092744.1:p.Thr275=
NM_012461.2:c.825T>G	NP_036593.2:p.Thr275=
XM_005267528.2:c.825T>G	XP_005267585.1:p.Thr275=
XM_005267529.2:c.720T>G	XP_005267586.1:p.Thr240=
NM_001099274.2:c.825T>G	NP_001092744.1:p.Thr275=
NM_001363668.1:c.720T>G	NP_001350597.1:p.Thr240=
NM_012461.3:c.825T>G	NP_036593.2:p.Thr275=
XM_011536642.2:c.*205T>G	XP_011534944.1:n.*205T>G
XM_017021216.2:c.183T>G	XP_016876705.1:p.Thr61=
XM_017021217.1:c.183T>G	XP_016876706.1:p.Thr61=
NM_001099274.3:c.825T>G MANE Select	NP_001092744.1:p.Thr275=
NM_001363668.2:c.720T>G	NP_001350597.1:p.Thr240=