Canonical Allele Identifier: CA2123849002

Gene: TINF2

Linked Data

• dbSNP Id: rs2040543704

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240341A>G , CM000676.2:g.24240341A>G	GRCh38
NC_000014.8:g.24709547A>G , CM000676.1:g.24709547A>G	GRCh37
NC_000014.7:g.23779387A>G	NCBI36
NG_016650.1:g.7334T>C
NG_054634.1:g.12925A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1442T>C
ENST00000557921.3:c.*74T>C	ENSP00000453157.3:n.*74T>C
ENST00000699682.1:n.1529T>C
ENST00000699683.1:n.1579T>C
ENST00000699684.1:c.*732T>C	ENSP00000514523.1:n.*732T>C
ENST00000699685.1:n.1343T>C
ENST00000699686.1:c.*74T>C	ENSP00000514524.1:n.*74T>C
ENST00000699687.1:c.*74T>C	ENSP00000514525.1:n.*74T>C
ENST00000699688.1:n.1339T>C
ENST00000699689.1:n.1695T>C
ENST00000699690.1:n.1892T>C
ENST00000699691.1:n.2036T>C
ENST00000699693.1:n.1479-11T>C
ENST00000699694.1:n.1798T>C
ENST00000699695.1:c.*434-11T>C	ENSP00000514526.1:n.*434-11T>C
ENST00000699696.1:n.1442T>C
ENST00000699697.1:c.1062-11T>C	ENSP00000514527.1:n.1062-11T>C
ENST00000699698.1:n.983-11T>C
ENST00000699699.1:n.1463T>C
ENST00000699700.1:n.1586T>C
ENST00000699701.1:c.*519T>C	ENSP00000514528.1:n.*519T>C
ENST00000267415.12:c.1062-11T>C MANE Select	ENSP00000267415.7:n.1062-11T>C
ENST00000646753.1:c.957-11T>C	ENSP00000494065.1:n.957-11T>C
ENST00000267415.11:c.1062-11T>C	ENSP00000267415.7:n.1062-11T>C
ENST00000399423.8:c.*74T>C	ENSP00000382350.4:n.*74T>C
ENST00000557915.1:n.258T>C
ENST00000558566.1:c.*511T>C	ENSP00000453025.1:n.*511T>C
ENST00000559969.5:c.897T>C
ENST00000560019.5:c.57-11T>C	ENSP00000453113.1:n.57-11T>C
ENST00000626689.2:c.*434-11T>C	ENSP00000486681.1:n.*434-11T>C
NM_001099274.1:c.1062-11T>C	NP_001092744.1:n.1062-11T>C
NM_012461.2:c.*74T>C	NP_036593.2:n.*74T>C
XM_005267528.2:c.1062-11T>C	XP_005267585.1:n.1062-11T>C
XM_005267529.2:c.957-11T>C	XP_005267586.1:n.957-11T>C
NM_001099274.2:c.1062-11T>C	NP_001092744.1:n.1062-11T>C
NM_001363668.1:c.957-11T>C	NP_001350597.1:n.957-11T>C
NM_012461.3:c.*74T>C	NP_036593.2:n.*74T>C
XM_011536642.2:c.*519T>C	XP_011534944.1:n.*519T>C
XM_017021216.2:c.420-11T>C	XP_016876705.1:n.420-11T>C
XM_017021217.1:c.420-11T>C	XP_016876706.1:n.420-11T>C
NM_001099274.3:c.1062-11T>C MANE Select	NP_001092744.1:n.1062-11T>C
NM_001363668.2:c.957-11T>C	NP_001350597.1:n.957-11T>C