Canonical Allele Identifier: CA613320515

Gene: TINF2

Linked Data

• dbSNP Id: rs1311746563
• gnomAD v2: 14-24709448-A-T
• gnomAD v4: 14-24240242-A-T
• MyVariant Identifiers: chr14:g.24709448A>T (hg19) ; chr14:g.24240242A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240242A>T , CM000676.2:g.24240242A>T	GRCh38
NC_000014.8:g.24709448A>T , CM000676.1:g.24709448A>T	GRCh37
NC_000014.7:g.23779288A>T	NCBI36
NG_016650.1:g.7433T>A
NG_054634.1:g.12826A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1520+21T>A
ENST00000557921.3:c.*173T>A	ENSP00000453157.3:n.*173T>A
ENST00000699682.1:n.1628T>A
ENST00000699683.1:n.1678T>A
ENST00000699684.1:c.*831T>A	ENSP00000514523.1:n.*831T>A
ENST00000699685.1:n.1442T>A
ENST00000699686.1:c.*173T>A	ENSP00000514524.1:n.*173T>A
ENST00000699687.1:c.*173T>A	ENSP00000514525.1:n.*173T>A
ENST00000699688.1:n.1438T>A
ENST00000699689.1:n.1794T>A
ENST00000699690.1:n.1991T>A
ENST00000699691.1:n.2135T>A
ENST00000699692.1:n.68+21T>A
ENST00000699693.1:n.1546+21T>A
ENST00000699694.1:n.1897T>A
ENST00000699695.1:c.*501+21T>A	ENSP00000514526.1:n.*501+21T>A
ENST00000699696.1:n.1520+21T>A
ENST00000699697.1:c.*13T>A	ENSP00000514527.1:n.*13T>A
ENST00000699698.1:n.1071T>A
ENST00000699699.1:n.1562T>A
ENST00000699700.1:n.1685T>A
ENST00000699701.1:c.*618T>A	ENSP00000514528.1:n.*618T>A
ENST00000267415.12:c.1129+21T>A MANE Select	ENSP00000267415.7:n.1129+21T>A
ENST00000646753.1:c.1024+21T>A	ENSP00000494065.1:n.1024+21T>A
ENST00000267415.11:c.1129+21T>A	ENSP00000267415.7:n.1129+21T>A
ENST00000399423.8:c.*173T>A	ENSP00000382350.4:n.*173T>A
ENST00000557915.1:n.336+21T>A
ENST00000558566.1:c.*610T>A	ENSP00000453025.1:n.*610T>A
ENST00000558703.1:n.1T>A
ENST00000559969.5:c.996T>A
ENST00000560019.5:c.124+21T>A	ENSP00000453113.1:n.124+21T>A
ENST00000626689.2:c.*501+21T>A	ENSP00000486681.1:n.*501+21T>A
NM_001099274.1:c.1129+21T>A	NP_001092744.1:n.1129+21T>A
NM_012461.2:c.*173T>A	NP_036593.2:n.*173T>A
XM_005267528.2:c.1129+21T>A	XP_005267585.1:n.1129+21T>A
XM_005267529.2:c.1024+21T>A	XP_005267586.1:n.1024+21T>A
NM_001099274.2:c.1129+21T>A	NP_001092744.1:n.1129+21T>A
NM_001363668.1:c.1024+21T>A	NP_001350597.1:n.1024+21T>A
NM_012461.3:c.*173T>A	NP_036593.2:n.*173T>A
XM_011536642.2:c.*618T>A	XP_011534944.1:n.*618T>A
XM_017021216.2:c.487+21T>A	XP_016876705.1:n.487+21T>A
XM_017021217.1:c.487+21T>A	XP_016876706.1:n.487+21T>A
NM_001099274.3:c.1129+21T>A MANE Select	NP_001092744.1:n.1129+21T>A
NM_001363668.2:c.1024+21T>A	NP_001350597.1:n.1024+21T>A