Canonical Allele Identifier: CA389225332

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709820G>C (hg19) ; chr14:g.24240614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240614G>C , CM000676.2:g.24240614G>C	GRCh38
NC_000014.8:g.24709820G>C , CM000676.1:g.24709820G>C	GRCh37
NC_000014.7:g.23779660G>C	NCBI36
NG_016650.1:g.7061C>G
NG_054634.1:g.13198G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1169C>G
ENST00000557921.3:c.758C>G	ENSP00000453157.3:p.Pro253Arg
ENST00000699682.1:n.1256C>G
ENST00000699683.1:n.1306C>G
ENST00000699684.1:c.*459C>G	ENSP00000514523.1:n.*459C>G
ENST00000699685.1:n.1070C>G
ENST00000699686.1:c.659C>G	ENSP00000514524.1:p.Pro220Arg
ENST00000699687.1:c.761C>G	ENSP00000514525.1:p.Pro254Arg
ENST00000699688.1:n.1066C>G
ENST00000699689.1:n.1422C>G
ENST00000699690.1:n.1619C>G
ENST00000699691.1:n.1763C>G
ENST00000699693.1:n.1283C>G
ENST00000699694.1:n.1525C>G
ENST00000699695.1:c.*238C>G	ENSP00000514526.1:n.*238C>G
ENST00000699696.1:n.1169C>G
ENST00000699697.1:c.866C>G	ENSP00000514527.1:p.Pro289Arg
ENST00000699698.1:n.787C>G
ENST00000699699.1:n.1190C>G
ENST00000699700.1:n.1313C>G
ENST00000699701.1:c.*246C>G	ENSP00000514528.1:n.*246C>G
ENST00000267415.12:c.866C>G MANE Select	ENSP00000267415.7:p.Pro289Arg
ENST00000557921.2:c.758C>G	ENSP00000453157.2:p.Pro253Arg
ENST00000646753.1:c.761C>G	ENSP00000494065.1:p.Pro254Arg
ENST00000267415.11:c.866C>G	ENSP00000267415.7:p.Pro289Arg
ENST00000399423.8:c.866C>G	ENSP00000382350.4:p.Pro289Arg
ENST00000558476.5:c.428C>G	ENSP00000452724.1:p.Pro143Arg
ENST00000558566.1:c.*238C>G	ENSP00000453025.1:n.*238C>G
ENST00000559019.1:c.*238C>G	ENSP00000453675.1:n.*238C>G
ENST00000559549.1:n.592C>G
ENST00000559969.5:c.757+65C>G
ENST00000626689.2:c.*238C>G	ENSP00000486681.1:n.*238C>G
NM_001099274.1:c.866C>G	NP_001092744.1:p.Pro289Arg
NM_012461.2:c.866C>G	NP_036593.2:p.Pro289Arg
XM_005267528.2:c.866C>G	XP_005267585.1:p.Pro289Arg
XM_005267529.2:c.761C>G	XP_005267586.1:p.Pro254Arg
NM_001099274.2:c.866C>G	NP_001092744.1:p.Pro289Arg
NM_001363668.1:c.761C>G	NP_001350597.1:p.Pro254Arg
NM_012461.3:c.866C>G	NP_036593.2:p.Pro289Arg
XM_011536642.2:c.*246C>G	XP_011534944.1:n.*246C>G
XM_017021216.2:c.224C>G	XP_016876705.1:p.Pro75Arg
XM_017021217.1:c.224C>G	XP_016876706.1:p.Pro75Arg
NM_001099274.3:c.866C>G MANE Select	NP_001092744.1:p.Pro289Arg
NM_001363668.2:c.761C>G	NP_001350597.1:p.Pro254Arg