Canonical Allele Identifier: CA389225117

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709799G>C (hg19) ; chr14:g.24240593G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240593G>C , CM000676.2:g.24240593G>C	GRCh38
NC_000014.8:g.24709799G>C , CM000676.1:g.24709799G>C	GRCh37
NC_000014.7:g.23779639G>C	NCBI36
NG_016650.1:g.7082C>G
NG_054634.1:g.13177G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1190C>G
ENST00000557921.3:c.779C>G	ENSP00000453157.3:p.Pro260Arg
ENST00000699682.1:n.1277C>G
ENST00000699683.1:n.1327C>G
ENST00000699684.1:c.*480C>G	ENSP00000514523.1:n.*480C>G
ENST00000699685.1:n.1091C>G
ENST00000699686.1:c.680C>G	ENSP00000514524.1:p.Pro227Arg
ENST00000699687.1:c.782C>G	ENSP00000514525.1:p.Pro261Arg
ENST00000699688.1:n.1087C>G
ENST00000699689.1:n.1443C>G
ENST00000699690.1:n.1640C>G
ENST00000699691.1:n.1784C>G
ENST00000699693.1:n.1304C>G
ENST00000699694.1:n.1546C>G
ENST00000699695.1:c.*259C>G	ENSP00000514526.1:n.*259C>G
ENST00000699696.1:n.1190C>G
ENST00000699697.1:c.887C>G	ENSP00000514527.1:p.Pro296Arg
ENST00000699698.1:n.808C>G
ENST00000699699.1:n.1211C>G
ENST00000699700.1:n.1334C>G
ENST00000699701.1:c.*267C>G	ENSP00000514528.1:n.*267C>G
ENST00000267415.12:c.887C>G MANE Select	ENSP00000267415.7:p.Pro296Arg
ENST00000557921.2:c.779C>G	ENSP00000453157.2:p.Pro260Arg
ENST00000646753.1:c.782C>G	ENSP00000494065.1:p.Pro261Arg
ENST00000267415.11:c.887C>G	ENSP00000267415.7:p.Pro296Arg
ENST00000399423.8:c.887C>G	ENSP00000382350.4:p.Pro296Arg
ENST00000557915.1:n.6C>G
ENST00000558566.1:c.*259C>G	ENSP00000453025.1:n.*259C>G
ENST00000559019.1:c.*259C>G	ENSP00000453675.1:n.*259C>G
ENST00000559549.1:n.613C>G
ENST00000559969.5:c.757+86C>G
ENST00000626689.2:c.*259C>G	ENSP00000486681.1:n.*259C>G
NM_001099274.1:c.887C>G	NP_001092744.1:p.Pro296Arg
NM_012461.2:c.887C>G	NP_036593.2:p.Pro296Arg
XM_005267528.2:c.887C>G	XP_005267585.1:p.Pro296Arg
XM_005267529.2:c.782C>G	XP_005267586.1:p.Pro261Arg
NM_001099274.2:c.887C>G	NP_001092744.1:p.Pro296Arg
NM_001363668.1:c.782C>G	NP_001350597.1:p.Pro261Arg
NM_012461.3:c.887C>G	NP_036593.2:p.Pro296Arg
XM_011536642.2:c.*267C>G	XP_011534944.1:n.*267C>G
XM_017021216.2:c.245C>G	XP_016876705.1:p.Pro82Arg
XM_017021217.1:c.245C>G	XP_016876706.1:p.Pro82Arg
NM_001099274.3:c.887C>G MANE Select	NP_001092744.1:p.Pro296Arg
NM_001363668.2:c.782C>G	NP_001350597.1:p.Pro261Arg