Canonical Allele Identifier: CA485782117

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709810A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240604A>G , CM000676.2:g.24240604A>G	GRCh38
NC_000014.8:g.24709810A>G , CM000676.1:g.24709810A>G	GRCh37
NC_000014.7:g.23779650A>G	NCBI36
NG_016650.1:g.7071T>C
NG_054634.1:g.13188A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1179T>C
ENST00000557921.3:c.768T>C	ENSP00000453157.3:p.Asn256=
ENST00000699682.1:n.1266T>C
ENST00000699683.1:n.1316T>C
ENST00000699684.1:c.*469T>C	ENSP00000514523.1:n.*469T>C
ENST00000699685.1:n.1080T>C
ENST00000699686.1:c.669T>C	ENSP00000514524.1:p.Asn223=
ENST00000699687.1:c.771T>C	ENSP00000514525.1:p.Asn257=
ENST00000699688.1:n.1076T>C
ENST00000699689.1:n.1432T>C
ENST00000699690.1:n.1629T>C
ENST00000699691.1:n.1773T>C
ENST00000699693.1:n.1293T>C
ENST00000699694.1:n.1535T>C
ENST00000699695.1:c.*248T>C	ENSP00000514526.1:n.*248T>C
ENST00000699696.1:n.1179T>C
ENST00000699697.1:c.876T>C	ENSP00000514527.1:p.Asn292=
ENST00000699698.1:n.797T>C
ENST00000699699.1:n.1200T>C
ENST00000699700.1:n.1323T>C
ENST00000699701.1:c.*256T>C	ENSP00000514528.1:n.*256T>C
ENST00000267415.12:c.876T>C MANE Select	ENSP00000267415.7:p.Asn292=
ENST00000557921.2:c.768T>C	ENSP00000453157.2:p.Asn256=
ENST00000646753.1:c.771T>C	ENSP00000494065.1:p.Asn257=
ENST00000267415.11:c.876T>C	ENSP00000267415.7:p.Asn292=
ENST00000399423.8:c.876T>C	ENSP00000382350.4:p.Asn292=
ENST00000558476.5:c.438T>C	ENSP00000452724.1:p.Asn146=
ENST00000558566.1:c.*248T>C	ENSP00000453025.1:n.*248T>C
ENST00000559019.1:c.*248T>C	ENSP00000453675.1:n.*248T>C
ENST00000559549.1:n.602T>C
ENST00000559969.5:c.757+75T>C
ENST00000626689.2:c.*248T>C	ENSP00000486681.1:n.*248T>C
NM_001099274.1:c.876T>C	NP_001092744.1:p.Asn292=
NM_012461.2:c.876T>C	NP_036593.2:p.Asn292=
XM_005267528.2:c.876T>C	XP_005267585.1:p.Asn292=
XM_005267529.2:c.771T>C	XP_005267586.1:p.Asn257=
NM_001099274.2:c.876T>C	NP_001092744.1:p.Asn292=
NM_001363668.1:c.771T>C	NP_001350597.1:p.Asn257=
NM_012461.3:c.876T>C	NP_036593.2:p.Asn292=
XM_011536642.2:c.*256T>C	XP_011534944.1:n.*256T>C
XM_017021216.2:c.234T>C	XP_016876705.1:p.Asn78=
XM_017021217.1:c.234T>C	XP_016876706.1:p.Asn78=
NM_001099274.3:c.876T>C MANE Select	NP_001092744.1:p.Asn292=
NM_001363668.2:c.771T>C	NP_001350597.1:p.Asn257=