Canonical Allele Identifier: CA485782101

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709801T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240595T>G , CM000676.2:g.24240595T>G	GRCh38
NC_000014.8:g.24709801T>G , CM000676.1:g.24709801T>G	GRCh37
NC_000014.7:g.23779641T>G	NCBI36
NG_016650.1:g.7080A>C
NG_054634.1:g.13179T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1188A>C
ENST00000557921.3:c.777A>C	ENSP00000453157.3:p.Ser259=
ENST00000699682.1:n.1275A>C
ENST00000699683.1:n.1325A>C
ENST00000699684.1:c.*478A>C	ENSP00000514523.1:n.*478A>C
ENST00000699685.1:n.1089A>C
ENST00000699686.1:c.678A>C	ENSP00000514524.1:p.Ser226=
ENST00000699687.1:c.780A>C	ENSP00000514525.1:p.Ser260=
ENST00000699688.1:n.1085A>C
ENST00000699689.1:n.1441A>C
ENST00000699690.1:n.1638A>C
ENST00000699691.1:n.1782A>C
ENST00000699693.1:n.1302A>C
ENST00000699694.1:n.1544A>C
ENST00000699695.1:c.*257A>C	ENSP00000514526.1:n.*257A>C
ENST00000699696.1:n.1188A>C
ENST00000699697.1:c.885A>C	ENSP00000514527.1:p.Ser295=
ENST00000699698.1:n.806A>C
ENST00000699699.1:n.1209A>C
ENST00000699700.1:n.1332A>C
ENST00000699701.1:c.*265A>C	ENSP00000514528.1:n.*265A>C
ENST00000267415.12:c.885A>C MANE Select	ENSP00000267415.7:p.Ser295=
ENST00000557921.2:c.777A>C	ENSP00000453157.2:p.Ser259=
ENST00000646753.1:c.780A>C	ENSP00000494065.1:p.Ser260=
ENST00000267415.11:c.885A>C	ENSP00000267415.7:p.Ser295=
ENST00000399423.8:c.885A>C	ENSP00000382350.4:p.Ser295=
ENST00000557915.1:n.4A>C
ENST00000558566.1:c.*257A>C	ENSP00000453025.1:n.*257A>C
ENST00000559019.1:c.*257A>C	ENSP00000453675.1:n.*257A>C
ENST00000559549.1:n.611A>C
ENST00000559969.5:c.757+84A>C
ENST00000626689.2:c.*257A>C	ENSP00000486681.1:n.*257A>C
NM_001099274.1:c.885A>C	NP_001092744.1:p.Ser295=
NM_012461.2:c.885A>C	NP_036593.2:p.Ser295=
XM_005267528.2:c.885A>C	XP_005267585.1:p.Ser295=
XM_005267529.2:c.780A>C	XP_005267586.1:p.Ser260=
NM_001099274.2:c.885A>C	NP_001092744.1:p.Ser295=
NM_001363668.1:c.780A>C	NP_001350597.1:p.Ser260=
NM_012461.3:c.885A>C	NP_036593.2:p.Ser295=
XM_011536642.2:c.*265A>C	XP_011534944.1:n.*265A>C
XM_017021216.2:c.243A>C	XP_016876705.1:p.Ser81=
XM_017021217.1:c.243A>C	XP_016876706.1:p.Ser81=
NM_001099274.3:c.885A>C MANE Select	NP_001092744.1:p.Ser295=
NM_001363668.2:c.780A>C	NP_001350597.1:p.Ser260=