Canonical Allele Identifier: CA485782155

Gene: TINF2

Linked Data

• gnomAD v4: 14-24240652-C-T
• MyVariant Identifiers: chr14:g.24709858C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240652C>T , CM000676.2:g.24240652C>T	GRCh38
NC_000014.8:g.24709858C>T , CM000676.1:g.24709858C>T	GRCh37
NC_000014.7:g.23779698C>T	NCBI36
NG_016650.1:g.7023G>A
NG_054634.1:g.13236C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1131G>A
ENST00000557921.3:c.720G>A	ENSP00000453157.3:p.Arg240=
ENST00000699682.1:n.1218G>A
ENST00000699683.1:n.1268G>A
ENST00000699684.1:c.*421G>A	ENSP00000514523.1:n.*421G>A
ENST00000699685.1:n.1032G>A
ENST00000699686.1:c.621G>A	ENSP00000514524.1:p.Arg207=
ENST00000699687.1:c.723G>A	ENSP00000514525.1:p.Arg241=
ENST00000699688.1:n.1028G>A
ENST00000699689.1:n.1384G>A
ENST00000699690.1:n.1581G>A
ENST00000699691.1:n.1725G>A
ENST00000699693.1:n.1245G>A
ENST00000699694.1:n.1487G>A
ENST00000699695.1:c.*200G>A	ENSP00000514526.1:n.*200G>A
ENST00000699696.1:n.1131G>A
ENST00000699697.1:c.828G>A	ENSP00000514527.1:p.Arg276=
ENST00000699698.1:n.749G>A
ENST00000699699.1:n.1152G>A
ENST00000699700.1:n.1275G>A
ENST00000699701.1:c.*208G>A	ENSP00000514528.1:n.*208G>A
ENST00000267415.12:c.828G>A MANE Select	ENSP00000267415.7:p.Arg276=
ENST00000557921.2:c.720G>A	ENSP00000453157.2:p.Arg240=
ENST00000646753.1:c.723G>A	ENSP00000494065.1:p.Arg241=
ENST00000267415.11:c.828G>A	ENSP00000267415.7:p.Arg276=
ENST00000399423.8:c.828G>A	ENSP00000382350.4:p.Arg276=
ENST00000558476.5:c.390G>A	ENSP00000452724.1:p.Arg130=
ENST00000558566.1:c.*200G>A	ENSP00000453025.1:n.*200G>A
ENST00000559019.1:c.*200G>A	ENSP00000453675.1:n.*200G>A
ENST00000559549.1:n.554G>A
ENST00000559969.5:c.757+27G>A
ENST00000626689.2:c.*200G>A	ENSP00000486681.1:n.*200G>A
NM_001099274.1:c.828G>A	NP_001092744.1:p.Arg276=
NM_012461.2:c.828G>A	NP_036593.2:p.Arg276=
XM_005267528.2:c.828G>A	XP_005267585.1:p.Arg276=
XM_005267529.2:c.723G>A	XP_005267586.1:p.Arg241=
NM_001099274.2:c.828G>A	NP_001092744.1:p.Arg276=
NM_001363668.1:c.723G>A	NP_001350597.1:p.Arg241=
NM_012461.3:c.828G>A	NP_036593.2:p.Arg276=
XM_011536642.2:c.*208G>A	XP_011534944.1:n.*208G>A
XM_017021216.2:c.186G>A	XP_016876705.1:p.Arg62=
XM_017021217.1:c.186G>A	XP_016876706.1:p.Arg62=
NM_001099274.3:c.828G>A MANE Select	NP_001092744.1:p.Arg276=
NM_001363668.2:c.723G>A	NP_001350597.1:p.Arg241=