Canonical Allele Identifier: CA389225256

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709812T>A (hg19) ; chr14:g.24240606T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240606T>A , CM000676.2:g.24240606T>A	GRCh38
NC_000014.8:g.24709812T>A , CM000676.1:g.24709812T>A	GRCh37
NC_000014.7:g.23779652T>A	NCBI36
NG_016650.1:g.7069A>T
NG_054634.1:g.13190T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1177A>T
ENST00000557921.3:c.766A>T	ENSP00000453157.3:p.Asn256Tyr
ENST00000699682.1:n.1264A>T
ENST00000699683.1:n.1314A>T
ENST00000699684.1:c.*467A>T	ENSP00000514523.1:n.*467A>T
ENST00000699685.1:n.1078A>T
ENST00000699686.1:c.667A>T	ENSP00000514524.1:p.Asn223Tyr
ENST00000699687.1:c.769A>T	ENSP00000514525.1:p.Asn257Tyr
ENST00000699688.1:n.1074A>T
ENST00000699689.1:n.1430A>T
ENST00000699690.1:n.1627A>T
ENST00000699691.1:n.1771A>T
ENST00000699693.1:n.1291A>T
ENST00000699694.1:n.1533A>T
ENST00000699695.1:c.*246A>T	ENSP00000514526.1:n.*246A>T
ENST00000699696.1:n.1177A>T
ENST00000699697.1:c.874A>T	ENSP00000514527.1:p.Asn292Tyr
ENST00000699698.1:n.795A>T
ENST00000699699.1:n.1198A>T
ENST00000699700.1:n.1321A>T
ENST00000699701.1:c.*254A>T	ENSP00000514528.1:n.*254A>T
ENST00000267415.12:c.874A>T MANE Select	ENSP00000267415.7:p.Asn292Tyr
ENST00000557921.2:c.766A>T	ENSP00000453157.2:p.Asn256Tyr
ENST00000646753.1:c.769A>T	ENSP00000494065.1:p.Asn257Tyr
ENST00000267415.11:c.874A>T	ENSP00000267415.7:p.Asn292Tyr
ENST00000399423.8:c.874A>T	ENSP00000382350.4:p.Asn292Tyr
ENST00000558476.5:c.436A>T	ENSP00000452724.1:p.Asn146Tyr
ENST00000558566.1:c.*246A>T	ENSP00000453025.1:n.*246A>T
ENST00000559019.1:c.*246A>T	ENSP00000453675.1:n.*246A>T
ENST00000559549.1:n.600A>T
ENST00000559969.5:c.757+73A>T
ENST00000626689.2:c.*246A>T	ENSP00000486681.1:n.*246A>T
NM_001099274.1:c.874A>T	NP_001092744.1:p.Asn292Tyr
NM_012461.2:c.874A>T	NP_036593.2:p.Asn292Tyr
XM_005267528.2:c.874A>T	XP_005267585.1:p.Asn292Tyr
XM_005267529.2:c.769A>T	XP_005267586.1:p.Asn257Tyr
NM_001099274.2:c.874A>T	NP_001092744.1:p.Asn292Tyr
NM_001363668.1:c.769A>T	NP_001350597.1:p.Asn257Tyr
NM_012461.3:c.874A>T	NP_036593.2:p.Asn292Tyr
XM_011536642.2:c.*254A>T	XP_011534944.1:n.*254A>T
XM_017021216.2:c.232A>T	XP_016876705.1:p.Asn78Tyr
XM_017021217.1:c.232A>T	XP_016876706.1:p.Asn78Tyr
NM_001099274.3:c.874A>T MANE Select	NP_001092744.1:p.Asn292Tyr
NM_001363668.2:c.769A>T	NP_001350597.1:p.Asn257Tyr