Canonical Allele Identifier: CA389223528

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709649T>C (hg19) ; chr14:g.24240443T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240443T>C , CM000676.2:g.24240443T>C	GRCh38
NC_000014.8:g.24709649T>C , CM000676.1:g.24709649T>C	GRCh37
NC_000014.7:g.23779489T>C	NCBI36
NG_016650.1:g.7232A>G
NG_054634.1:g.13027T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1340A>G
ENST00000557921.3:c.929A>G	ENSP00000453157.3:p.Asp310Gly
ENST00000699682.1:n.1427A>G
ENST00000699683.1:n.1477A>G
ENST00000699684.1:c.*630A>G	ENSP00000514523.1:n.*630A>G
ENST00000699685.1:n.1241A>G
ENST00000699686.1:c.830A>G	ENSP00000514524.1:p.Asp277Gly
ENST00000699687.1:c.932A>G	ENSP00000514525.1:p.Asp311Gly
ENST00000699688.1:n.1237A>G
ENST00000699689.1:n.1593A>G
ENST00000699690.1:n.1790A>G
ENST00000699691.1:n.1934A>G
ENST00000699693.1:n.1454A>G
ENST00000699694.1:n.1696A>G
ENST00000699695.1:c.*409A>G	ENSP00000514526.1:n.*409A>G
ENST00000699696.1:n.1340A>G
ENST00000699697.1:c.1037A>G	ENSP00000514527.1:p.Asp346Gly
ENST00000699698.1:n.958A>G
ENST00000699699.1:n.1361A>G
ENST00000699700.1:n.1484A>G
ENST00000699701.1:c.*417A>G	ENSP00000514528.1:n.*417A>G
ENST00000267415.12:c.1037A>G MANE Select	ENSP00000267415.7:p.Asp346Gly
ENST00000646753.1:c.932A>G	ENSP00000494065.1:p.Asp311Gly
ENST00000267415.11:c.1037A>G	ENSP00000267415.7:p.Asp346Gly
ENST00000399423.8:c.1037A>G	ENSP00000382350.4:p.Asp346Gly
ENST00000557915.1:n.156A>G
ENST00000558566.1:c.*409A>G	ENSP00000453025.1:n.*409A>G
ENST00000559969.5:c.795A>G
ENST00000560019.5:c.32A>G	ENSP00000453113.1:p.Asp11Gly
ENST00000626689.2:c.*409A>G	ENSP00000486681.1:n.*409A>G
NM_001099274.1:c.1037A>G	NP_001092744.1:p.Asp346Gly
NM_012461.2:c.1037A>G	NP_036593.2:p.Asp346Gly
XM_005267528.2:c.1037A>G	XP_005267585.1:p.Asp346Gly
XM_005267529.2:c.932A>G	XP_005267586.1:p.Asp311Gly
NM_001099274.2:c.1037A>G	NP_001092744.1:p.Asp346Gly
NM_001363668.1:c.932A>G	NP_001350597.1:p.Asp311Gly
NM_012461.3:c.1037A>G	NP_036593.2:p.Asp346Gly
XM_011536642.2:c.*417A>G	XP_011534944.1:n.*417A>G
XM_017021216.2:c.395A>G	XP_016876705.1:p.Asp132Gly
XM_017021217.1:c.395A>G	XP_016876706.1:p.Asp132Gly
NM_001099274.3:c.1037A>G MANE Select	NP_001092744.1:p.Asp346Gly
NM_001363668.2:c.932A>G	NP_001350597.1:p.Asp311Gly