Canonical Allele Identifier: CA7130483

Gene: TINF2

Linked Data

• dbSNP Id: rs759185690
• ExAC: 14:24709389 A / G
• gnomAD v2: 14-24709389-A-G
• MyVariant Identifiers: chr14:g.24709389A>G (hg19) ; chr14:g.24240183A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240183A>G , CM000676.2:g.24240183A>G	GRCh38
NC_000014.8:g.24709389A>G , CM000676.1:g.24709389A>G	GRCh37
NC_000014.7:g.23779229A>G	NCBI36
NG_016650.1:g.7492T>C
NG_054634.1:g.12767A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1521-28T>C
ENST00000557921.3:c.*232T>C	ENSP00000453157.3:n.*232T>C
ENST00000699682.1:n.1687T>C
ENST00000699683.1:n.1737T>C
ENST00000699684.1:c.*890T>C	ENSP00000514523.1:n.*890T>C
ENST00000699685.1:n.1501T>C
ENST00000699686.1:c.*232T>C	ENSP00000514524.1:n.*232T>C
ENST00000699687.1:c.*232T>C	ENSP00000514525.1:n.*232T>C
ENST00000699688.1:n.1497T>C
ENST00000699689.1:n.1853T>C
ENST00000699690.1:n.2050T>C
ENST00000699691.1:n.2194T>C
ENST00000699692.1:n.69T>C
ENST00000699693.1:n.1547-28T>C
ENST00000699694.1:n.1956T>C
ENST00000699695.1:c.*502-28T>C	ENSP00000514526.1:n.*502-28T>C
ENST00000699696.1:n.1521-28T>C
ENST00000699697.1:c.*72T>C	ENSP00000514527.1:n.*72T>C
ENST00000699698.1:n.1130T>C
ENST00000699699.1:n.1621T>C
ENST00000699700.1:n.1744T>C
ENST00000699701.1:c.*677T>C	ENSP00000514528.1:n.*677T>C
ENST00000267415.12:c.1130-28T>C MANE Select	ENSP00000267415.7:n.1130-28T>C
ENST00000646753.1:c.1025-28T>C	ENSP00000494065.1:n.1025-28T>C
ENST00000267415.11:c.1130-28T>C	ENSP00000267415.7:n.1130-28T>C
ENST00000399423.8:c.*232T>C	ENSP00000382350.4:n.*232T>C
ENST00000557915.1:n.337-28T>C
ENST00000558566.1:c.*669T>C	ENSP00000453025.1:n.*669T>C
ENST00000558703.1:n.60T>C
ENST00000559969.5:c.1055T>C
ENST00000560019.5:c.125-28T>C	ENSP00000453113.1:n.125-28T>C
ENST00000626689.2:c.*502-28T>C	ENSP00000486681.1:n.*502-28T>C
NM_001099274.1:c.1130-28T>C	NP_001092744.1:n.1130-28T>C
NM_012461.2:c.*232T>C	NP_036593.2:n.*232T>C
XM_005267528.2:c.1130-28T>C	XP_005267585.1:n.1130-28T>C
XM_005267529.2:c.1025-28T>C	XP_005267586.1:n.1025-28T>C
NM_001099274.2:c.1130-28T>C	NP_001092744.1:n.1130-28T>C
NM_001363668.1:c.1025-28T>C	NP_001350597.1:n.1025-28T>C
NM_012461.3:c.*232T>C	NP_036593.2:n.*232T>C
XM_011536642.2:c.*677T>C	XP_011534944.1:n.*677T>C
XM_017021216.2:c.488-28T>C	XP_016876705.1:n.488-28T>C
XM_017021217.1:c.488-28T>C	XP_016876706.1:n.488-28T>C
NM_001099274.3:c.1130-28T>C MANE Select	NP_001092744.1:n.1130-28T>C
NM_001363668.2:c.1025-28T>C	NP_001350597.1:n.1025-28T>C