Canonical Allele Identifier: CA389223098

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709531C>G (hg19) ; chr14:g.24240325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240325C>G , CM000676.2:g.24240325C>G	GRCh38
NC_000014.8:g.24709531C>G , CM000676.1:g.24709531C>G	GRCh37
NC_000014.7:g.23779371C>G	NCBI36
NG_016650.1:g.7350G>C
NG_054634.1:g.12909C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1458G>C
ENST00000557921.3:c.*90G>C	ENSP00000453157.3:n.*90G>C
ENST00000699682.1:n.1545G>C
ENST00000699683.1:n.1595G>C
ENST00000699684.1:c.*748G>C	ENSP00000514523.1:n.*748G>C
ENST00000699685.1:n.1359G>C
ENST00000699686.1:c.*90G>C	ENSP00000514524.1:n.*90G>C
ENST00000699687.1:c.*90G>C	ENSP00000514525.1:n.*90G>C
ENST00000699688.1:n.1355G>C
ENST00000699689.1:n.1711G>C
ENST00000699690.1:n.1908G>C
ENST00000699691.1:n.2052G>C
ENST00000699692.1:n.6G>C
ENST00000699693.1:n.1484G>C
ENST00000699694.1:n.1814G>C
ENST00000699695.1:c.*439G>C	ENSP00000514526.1:n.*439G>C
ENST00000699696.1:n.1458G>C
ENST00000699697.1:c.1067G>C	ENSP00000514527.1:p.Cys356Ser
ENST00000699698.1:n.988G>C
ENST00000699699.1:n.1479G>C
ENST00000699700.1:n.1602G>C
ENST00000699701.1:c.*535G>C	ENSP00000514528.1:n.*535G>C
ENST00000267415.12:c.1067G>C MANE Select	ENSP00000267415.7:p.Cys356Ser
ENST00000646753.1:c.962G>C	ENSP00000494065.1:p.Cys321Ser
ENST00000267415.11:c.1067G>C	ENSP00000267415.7:p.Cys356Ser
ENST00000399423.8:c.*90G>C	ENSP00000382350.4:n.*90G>C
ENST00000557915.1:n.274G>C
ENST00000558566.1:c.*527G>C	ENSP00000453025.1:n.*527G>C
ENST00000559969.5:c.913G>C
ENST00000560019.5:c.62G>C	ENSP00000453113.1:p.Cys21Ser
ENST00000626689.2:c.*439G>C	ENSP00000486681.1:n.*439G>C
NM_001099274.1:c.1067G>C	NP_001092744.1:p.Cys356Ser
NM_012461.2:c.*90G>C	NP_036593.2:n.*90G>C
XM_005267528.2:c.1067G>C	XP_005267585.1:p.Cys356Ser
XM_005267529.2:c.962G>C	XP_005267586.1:p.Cys321Ser
NM_001099274.2:c.1067G>C	NP_001092744.1:p.Cys356Ser
NM_001363668.1:c.962G>C	NP_001350597.1:p.Cys321Ser
NM_012461.3:c.*90G>C	NP_036593.2:n.*90G>C
XM_011536642.2:c.*535G>C	XP_011534944.1:n.*535G>C
XM_017021216.2:c.425G>C	XP_016876705.1:p.Cys142Ser
XM_017021217.1:c.425G>C	XP_016876706.1:p.Cys142Ser
NM_001099274.3:c.1067G>C MANE Select	NP_001092744.1:p.Cys356Ser
NM_001363668.2:c.962G>C	NP_001350597.1:p.Cys321Ser