Canonical Allele Identifier: CA485782110

Gene: TINF2

Linked Data

• ClinVar Variation Id: 1155962
• ClinVar RCV Id: RCV001498478
• dbSNP Id: rs1475173024
• gnomAD v2: 14-24709807-G-A
• gnomAD v4: 14-24240601-G-A
• COSMIC: COSM6025463 ; COSM6025464
• MyVariant Identifiers: chr14:g.24709807G>A (hg19) ; chr14:g.24240601G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240601G>A , CM000676.2:g.24240601G>A	GRCh38
NC_000014.8:g.24709807G>A , CM000676.1:g.24709807G>A	GRCh37
NC_000014.7:g.23779647G>A	NCBI36
NG_016650.1:g.7074C>T
NG_054634.1:g.13185G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1182C>T
ENST00000557921.3:c.771C>T	ENSP00000453157.3:p.Leu257=
ENST00000699682.1:n.1269C>T
ENST00000699683.1:n.1319C>T
ENST00000699684.1:c.*472C>T	ENSP00000514523.1:n.*472C>T
ENST00000699685.1:n.1083C>T
ENST00000699686.1:c.672C>T	ENSP00000514524.1:p.Leu224=
ENST00000699687.1:c.774C>T	ENSP00000514525.1:p.Leu258=
ENST00000699688.1:n.1079C>T
ENST00000699689.1:n.1435C>T
ENST00000699690.1:n.1632C>T
ENST00000699691.1:n.1776C>T
ENST00000699693.1:n.1296C>T
ENST00000699694.1:n.1538C>T
ENST00000699695.1:c.*251C>T	ENSP00000514526.1:n.*251C>T
ENST00000699696.1:n.1182C>T
ENST00000699697.1:c.879C>T	ENSP00000514527.1:p.Leu293=
ENST00000699698.1:n.800C>T
ENST00000699699.1:n.1203C>T
ENST00000699700.1:n.1326C>T
ENST00000699701.1:c.*259C>T	ENSP00000514528.1:n.*259C>T
ENST00000267415.12:c.879C>T MANE Select	ENSP00000267415.7:p.Leu293=
ENST00000557921.2:c.771C>T	ENSP00000453157.2:p.Leu257=
ENST00000646753.1:c.774C>T	ENSP00000494065.1:p.Leu258=
ENST00000267415.11:c.879C>T	ENSP00000267415.7:p.Leu293=
ENST00000399423.8:c.879C>T	ENSP00000382350.4:p.Leu293=
ENST00000558566.1:c.*251C>T	ENSP00000453025.1:n.*251C>T
ENST00000559019.1:c.*251C>T	ENSP00000453675.1:n.*251C>T
ENST00000559549.1:n.605C>T
ENST00000559969.5:c.757+78C>T
ENST00000626689.2:c.*251C>T	ENSP00000486681.1:n.*251C>T
NM_001099274.1:c.879C>T	NP_001092744.1:p.Leu293=
NM_012461.2:c.879C>T	NP_036593.2:p.Leu293=
XM_005267528.2:c.879C>T	XP_005267585.1:p.Leu293=
XM_005267529.2:c.774C>T	XP_005267586.1:p.Leu258=
NM_001099274.2:c.879C>T	NP_001092744.1:p.Leu293=
NM_001363668.1:c.774C>T	NP_001350597.1:p.Leu258=
NM_012461.3:c.879C>T	NP_036593.2:p.Leu293=
XM_011536642.2:c.*259C>T	XP_011534944.1:n.*259C>T
XM_017021216.2:c.237C>T	XP_016876705.1:p.Leu79=
XM_017021217.1:c.237C>T	XP_016876706.1:p.Leu79=
NM_001099274.3:c.879C>T MANE Select	NP_001092744.1:p.Leu293=
NM_001363668.2:c.774C>T	NP_001350597.1:p.Leu258=