Canonical Allele Identifier: CA485782233

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709900A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240694A>T , CM000676.2:g.24240694A>T	GRCh38
NC_000014.8:g.24709900A>T , CM000676.1:g.24709900A>T	GRCh37
NC_000014.7:g.23779740A>T	NCBI36
NG_016650.1:g.6981T>A
NG_054634.1:g.13278A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1089T>A
ENST00000557921.3:c.678T>A	ENSP00000453157.3:p.Pro226=
ENST00000699682.1:n.1176T>A
ENST00000699683.1:n.1226T>A
ENST00000699684.1:c.*379T>A	ENSP00000514523.1:n.*379T>A
ENST00000699685.1:n.990T>A
ENST00000699686.1:c.579T>A	ENSP00000514524.1:p.Pro193=
ENST00000699687.1:c.681T>A	ENSP00000514525.1:p.Pro227=
ENST00000699688.1:n.986T>A
ENST00000699689.1:n.1342T>A
ENST00000699690.1:n.1539T>A
ENST00000699691.1:n.1683T>A
ENST00000699693.1:n.1203T>A
ENST00000699694.1:n.1445T>A
ENST00000699695.1:c.*158T>A	ENSP00000514526.1:n.*158T>A
ENST00000699696.1:n.1089T>A
ENST00000699697.1:c.786T>A	ENSP00000514527.1:p.Pro262=
ENST00000699698.1:n.707T>A
ENST00000699699.1:n.1110T>A
ENST00000699700.1:n.1233T>A
ENST00000699701.1:c.*166T>A	ENSP00000514528.1:n.*166T>A
ENST00000267415.12:c.786T>A MANE Select	ENSP00000267415.7:p.Pro262=
ENST00000557921.2:c.678T>A	ENSP00000453157.2:p.Pro226=
ENST00000646753.1:c.681T>A	ENSP00000494065.1:p.Pro227=
ENST00000267415.11:c.786T>A	ENSP00000267415.7:p.Pro262=
ENST00000399423.8:c.786T>A	ENSP00000382350.4:p.Pro262=
ENST00000558476.5:c.348T>A	ENSP00000452724.1:p.Pro116=
ENST00000558566.1:c.*158T>A	ENSP00000453025.1:n.*158T>A
ENST00000559019.1:c.*158T>A	ENSP00000453675.1:n.*158T>A
ENST00000559549.1:n.512T>A
ENST00000559969.5:c.742T>A
ENST00000626689.2:c.*158T>A	ENSP00000486681.1:n.*158T>A
NM_001099274.1:c.786T>A	NP_001092744.1:p.Pro262=
NM_012461.2:c.786T>A	NP_036593.2:p.Pro262=
XM_005267528.2:c.786T>A	XP_005267585.1:p.Pro262=
XM_005267529.2:c.681T>A	XP_005267586.1:p.Pro227=
NM_001099274.2:c.786T>A	NP_001092744.1:p.Pro262=
NM_001363668.1:c.681T>A	NP_001350597.1:p.Pro227=
NM_012461.3:c.786T>A	NP_036593.2:p.Pro262=
XM_011536642.2:c.*166T>A	XP_011534944.1:n.*166T>A
XM_017021216.2:c.144T>A	XP_016876705.1:p.Pro48=
XM_017021217.1:c.144T>A	XP_016876706.1:p.Pro48=
NM_001099274.3:c.786T>A MANE Select	NP_001092744.1:p.Pro262=
NM_001363668.2:c.681T>A	NP_001350597.1:p.Pro227=