Canonical Allele Identifier: CA485782341

Gene: TINF2

Linked Data

• ClinVar Variation Id: 2029837
• ClinVar RCV Id: RCV002863879
• MyVariant Identifiers: chr14:g.24709972T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240766T>A , CM000676.2:g.24240766T>A	GRCh38
NC_000014.8:g.24709972T>A , CM000676.1:g.24709972T>A	GRCh37
NC_000014.7:g.23779812T>A	NCBI36
NG_016650.1:g.6909A>T
NG_054634.1:g.13350T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1017A>T
ENST00000557921.3:c.606A>T	ENSP00000453157.3:p.Thr202=
ENST00000699682.1:n.1104A>T
ENST00000699683.1:n.1154A>T
ENST00000699684.1:c.*307A>T	ENSP00000514523.1:n.*307A>T
ENST00000699685.1:n.918A>T
ENST00000699686.1:c.507A>T	ENSP00000514524.1:p.Thr169=
ENST00000699687.1:c.609A>T	ENSP00000514525.1:p.Thr203=
ENST00000699688.1:n.914A>T
ENST00000699689.1:n.1270A>T
ENST00000699690.1:n.1467A>T
ENST00000699691.1:n.1611A>T
ENST00000699693.1:n.1131A>T
ENST00000699694.1:n.1373A>T
ENST00000699695.1:c.*86A>T	ENSP00000514526.1:n.*86A>T
ENST00000699696.1:n.1017A>T
ENST00000699697.1:c.714A>T	ENSP00000514527.1:p.Thr238=
ENST00000699698.1:n.635A>T
ENST00000699699.1:n.1038A>T
ENST00000699700.1:n.1161A>T
ENST00000699701.1:c.*94A>T	ENSP00000514528.1:n.*94A>T
ENST00000267415.12:c.714A>T MANE Select	ENSP00000267415.7:p.Thr238=
ENST00000557921.2:c.606A>T	ENSP00000453157.2:p.Thr202=
ENST00000646753.1:c.609A>T	ENSP00000494065.1:p.Thr203=
ENST00000267415.11:c.714A>T	ENSP00000267415.7:p.Thr238=
ENST00000399423.8:c.714A>T	ENSP00000382350.4:p.Thr238=
ENST00000558476.5:c.276A>T	ENSP00000452724.1:p.Thr92=
ENST00000558566.1:c.*86A>T	ENSP00000453025.1:n.*86A>T
ENST00000559019.1:c.*86A>T	ENSP00000453675.1:n.*86A>T
ENST00000559549.1:n.440A>T
ENST00000559969.5:c.670A>T
ENST00000626689.2:c.*86A>T	ENSP00000486681.1:n.*86A>T
NM_001099274.1:c.714A>T	NP_001092744.1:p.Thr238=
NM_012461.2:c.714A>T	NP_036593.2:p.Thr238=
XM_005267528.2:c.714A>T	XP_005267585.1:p.Thr238=
XM_005267529.2:c.609A>T	XP_005267586.1:p.Thr203=
NM_001099274.2:c.714A>T	NP_001092744.1:p.Thr238=
NM_001363668.1:c.609A>T	NP_001350597.1:p.Thr203=
NM_012461.3:c.714A>T	NP_036593.2:p.Thr238=
XM_011536642.2:c.*94A>T	XP_011534944.1:n.*94A>T
XM_017021216.2:c.72A>T	XP_016876705.1:p.Thr24=
XM_017021217.1:c.72A>T	XP_016876706.1:p.Thr24=
NM_001099274.3:c.714A>T MANE Select	NP_001092744.1:p.Thr238=
NM_001363668.2:c.609A>T	NP_001350597.1:p.Thr203=