Canonical Allele Identifier: CA389223379

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709631T>G (hg19) ; chr14:g.24240425T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240425T>G , CM000676.2:g.24240425T>G	GRCh38
NC_000014.8:g.24709631T>G , CM000676.1:g.24709631T>G	GRCh37
NC_000014.7:g.23779471T>G	NCBI36
NG_016650.1:g.7250A>C
NG_054634.1:g.13009T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1358A>C
ENST00000557921.3:c.947A>C	ENSP00000453157.3:p.Gln316Pro
ENST00000699682.1:n.1445A>C
ENST00000699683.1:n.1495A>C
ENST00000699684.1:c.*648A>C	ENSP00000514523.1:n.*648A>C
ENST00000699685.1:n.1259A>C
ENST00000699686.1:c.848A>C	ENSP00000514524.1:p.Gln283Pro
ENST00000699687.1:c.950A>C	ENSP00000514525.1:p.Gln317Pro
ENST00000699688.1:n.1255A>C
ENST00000699689.1:n.1611A>C
ENST00000699690.1:n.1808A>C
ENST00000699691.1:n.1952A>C
ENST00000699693.1:n.1472A>C
ENST00000699694.1:n.1714A>C
ENST00000699695.1:c.*427A>C	ENSP00000514526.1:n.*427A>C
ENST00000699696.1:n.1358A>C
ENST00000699697.1:c.1055A>C	ENSP00000514527.1:p.Gln352Pro
ENST00000699698.1:n.976A>C
ENST00000699699.1:n.1379A>C
ENST00000699700.1:n.1502A>C
ENST00000699701.1:c.*435A>C	ENSP00000514528.1:n.*435A>C
ENST00000267415.12:c.1055A>C MANE Select	ENSP00000267415.7:p.Gln352Pro
ENST00000646753.1:c.950A>C	ENSP00000494065.1:p.Gln317Pro
ENST00000267415.11:c.1055A>C	ENSP00000267415.7:p.Gln352Pro
ENST00000399423.8:c.1055A>C	ENSP00000382350.4:p.Gln352Pro
ENST00000557915.1:n.174A>C
ENST00000558566.1:c.*427A>C	ENSP00000453025.1:n.*427A>C
ENST00000559969.5:c.813A>C
ENST00000560019.5:c.50A>C	ENSP00000453113.1:p.Gln17Pro
ENST00000626689.2:c.*427A>C	ENSP00000486681.1:n.*427A>C
NM_001099274.1:c.1055A>C	NP_001092744.1:p.Gln352Pro
NM_012461.2:c.1055A>C	NP_036593.2:p.Gln352Pro
XM_005267528.2:c.1055A>C	XP_005267585.1:p.Gln352Pro
XM_005267529.2:c.950A>C	XP_005267586.1:p.Gln317Pro
NM_001099274.2:c.1055A>C	NP_001092744.1:p.Gln352Pro
NM_001363668.1:c.950A>C	NP_001350597.1:p.Gln317Pro
NM_012461.3:c.1055A>C	NP_036593.2:p.Gln352Pro
XM_011536642.2:c.*435A>C	XP_011534944.1:n.*435A>C
XM_017021216.2:c.413A>C	XP_016876705.1:p.Gln138Pro
XM_017021217.1:c.413A>C	XP_016876706.1:p.Gln138Pro
NM_001099274.3:c.1055A>C MANE Select	NP_001092744.1:p.Gln352Pro
NM_001363668.2:c.950A>C	NP_001350597.1:p.Gln317Pro