Canonical Allele Identifier: CA485782249

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709678C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240472C>G , CM000676.2:g.24240472C>G	GRCh38
NC_000014.8:g.24709678C>G , CM000676.1:g.24709678C>G	GRCh37
NC_000014.7:g.23779518C>G	NCBI36
NG_016650.1:g.7203G>C
NG_054634.1:g.13056C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1311G>C
ENST00000557921.3:c.900G>C	ENSP00000453157.3:p.Gly300=
ENST00000699682.1:n.1398G>C
ENST00000699683.1:n.1448G>C
ENST00000699684.1:c.*601G>C	ENSP00000514523.1:n.*601G>C
ENST00000699685.1:n.1212G>C
ENST00000699686.1:c.801G>C	ENSP00000514524.1:p.Gly267=
ENST00000699687.1:c.903G>C	ENSP00000514525.1:p.Gly301=
ENST00000699688.1:n.1208G>C
ENST00000699689.1:n.1564G>C
ENST00000699690.1:n.1761G>C
ENST00000699691.1:n.1905G>C
ENST00000699693.1:n.1425G>C
ENST00000699694.1:n.1667G>C
ENST00000699695.1:c.*380G>C	ENSP00000514526.1:n.*380G>C
ENST00000699696.1:n.1311G>C
ENST00000699697.1:c.1008G>C	ENSP00000514527.1:p.Gly336=
ENST00000699698.1:n.929G>C
ENST00000699699.1:n.1332G>C
ENST00000699700.1:n.1455G>C
ENST00000699701.1:c.*388G>C	ENSP00000514528.1:n.*388G>C
ENST00000267415.12:c.1008G>C MANE Select	ENSP00000267415.7:p.Gly336=
ENST00000646753.1:c.903G>C	ENSP00000494065.1:p.Gly301=
ENST00000267415.11:c.1008G>C	ENSP00000267415.7:p.Gly336=
ENST00000399423.8:c.1008G>C	ENSP00000382350.4:p.Gly336=
ENST00000557915.1:n.127G>C
ENST00000558566.1:c.*380G>C	ENSP00000453025.1:n.*380G>C
ENST00000559969.5:c.766G>C
ENST00000560019.5:c.3G>C	ENSP00000453113.1:p.Gly1=
ENST00000626689.2:c.*380G>C	ENSP00000486681.1:n.*380G>C
NM_001099274.1:c.1008G>C	NP_001092744.1:p.Gly336=
NM_012461.2:c.1008G>C	NP_036593.2:p.Gly336=
XM_005267528.2:c.1008G>C	XP_005267585.1:p.Gly336=
XM_005267529.2:c.903G>C	XP_005267586.1:p.Gly301=
NM_001099274.2:c.1008G>C	NP_001092744.1:p.Gly336=
NM_001363668.1:c.903G>C	NP_001350597.1:p.Gly301=
NM_012461.3:c.1008G>C	NP_036593.2:p.Gly336=
XM_011536642.2:c.*388G>C	XP_011534944.1:n.*388G>C
XM_017021216.2:c.366G>C	XP_016876705.1:p.Gly122=
XM_017021217.1:c.366G>C	XP_016876706.1:p.Gly122=
NM_001099274.3:c.1008G>C MANE Select	NP_001092744.1:p.Gly336=
NM_001363668.2:c.903G>C	NP_001350597.1:p.Gly301=