Canonical Allele Identifier: CA389223693

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709672C>G (hg19) ; chr14:g.24240466C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240466C>G , CM000676.2:g.24240466C>G	GRCh38
NC_000014.8:g.24709672C>G , CM000676.1:g.24709672C>G	GRCh37
NC_000014.7:g.23779512C>G	NCBI36
NG_016650.1:g.7209G>C
NG_054634.1:g.13050C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1317G>C
ENST00000557921.3:c.906G>C	ENSP00000453157.3:p.Arg302Ser
ENST00000699682.1:n.1404G>C
ENST00000699683.1:n.1454G>C
ENST00000699684.1:c.*607G>C	ENSP00000514523.1:n.*607G>C
ENST00000699685.1:n.1218G>C
ENST00000699686.1:c.807G>C	ENSP00000514524.1:p.Arg269Ser
ENST00000699687.1:c.909G>C	ENSP00000514525.1:p.Arg303Ser
ENST00000699688.1:n.1214G>C
ENST00000699689.1:n.1570G>C
ENST00000699690.1:n.1767G>C
ENST00000699691.1:n.1911G>C
ENST00000699693.1:n.1431G>C
ENST00000699694.1:n.1673G>C
ENST00000699695.1:c.*386G>C	ENSP00000514526.1:n.*386G>C
ENST00000699696.1:n.1317G>C
ENST00000699697.1:c.1014G>C	ENSP00000514527.1:p.Arg338Ser
ENST00000699698.1:n.935G>C
ENST00000699699.1:n.1338G>C
ENST00000699700.1:n.1461G>C
ENST00000699701.1:c.*394G>C	ENSP00000514528.1:n.*394G>C
ENST00000267415.12:c.1014G>C MANE Select	ENSP00000267415.7:p.Arg338Ser
ENST00000646753.1:c.909G>C	ENSP00000494065.1:p.Arg303Ser
ENST00000267415.11:c.1014G>C	ENSP00000267415.7:p.Arg338Ser
ENST00000399423.8:c.1014G>C	ENSP00000382350.4:p.Arg338Ser
ENST00000557915.1:n.133G>C
ENST00000558566.1:c.*386G>C	ENSP00000453025.1:n.*386G>C
ENST00000559969.5:c.772G>C
ENST00000560019.5:c.9G>C	ENSP00000453113.1:p.Arg3Ser
ENST00000626689.2:c.*386G>C	ENSP00000486681.1:n.*386G>C
NM_001099274.1:c.1014G>C	NP_001092744.1:p.Arg338Ser
NM_012461.2:c.1014G>C	NP_036593.2:p.Arg338Ser
XM_005267528.2:c.1014G>C	XP_005267585.1:p.Arg338Ser
XM_005267529.2:c.909G>C	XP_005267586.1:p.Arg303Ser
NM_001099274.2:c.1014G>C	NP_001092744.1:p.Arg338Ser
NM_001363668.1:c.909G>C	NP_001350597.1:p.Arg303Ser
NM_012461.3:c.1014G>C	NP_036593.2:p.Arg338Ser
XM_011536642.2:c.*394G>C	XP_011534944.1:n.*394G>C
XM_017021216.2:c.372G>C	XP_016876705.1:p.Arg124Ser
XM_017021217.1:c.372G>C	XP_016876706.1:p.Arg124Ser
NM_001099274.3:c.1014G>C MANE Select	NP_001092744.1:p.Arg338Ser
NM_001363668.2:c.909G>C	NP_001350597.1:p.Arg303Ser