Canonical Allele Identifier: CA257883149

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24241471A>G , CM000676.2:g.24241471A>G	GRCh38
NC_000014.8:g.24710677A>G , CM000676.1:g.24710677A>G	GRCh37
NC_000014.7:g.23780517A>G	NCBI36
NG_016650.1:g.6204T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001099274.3:c.400-160T>C MANE Select	NP_001092744.1:n.400-160T>C
ENST00000267415.12:c.400-160T>C MANE Select	ENSP00000267415.7:n.400-160T>C
NM_001099274.1:c.400-160T>C	NP_001092744.1:n.400-160T>C
NM_001099274.2:c.400-160T>C	NP_001092744.1:n.400-160T>C
NM_001363668.1:c.295-160T>C	NP_001350597.1:n.295-160T>C
NM_001363668.2:c.295-160T>C	NP_001350597.1:n.295-160T>C
NM_012461.2:c.400-160T>C	NP_036593.2:n.400-160T>C
NM_012461.3:c.400-160T>C	NP_036593.2:n.400-160T>C
ENST00000267415.11:c.400-160T>C	ENSP00000267415.7:n.400-160T>C
ENST00000399423.8:c.400-160T>C	ENSP00000382350.4:n.400-160T>C
ENST00000557830.1:n.494T>C
ENST00000557915.2:n.703-160T>C
ENST00000557921.2:c.399+204T>C	ENSP00000453157.2:n.399+204T>C
ENST00000557921.3:c.399+204T>C	ENSP00000453157.3:n.399+204T>C
ENST00000558476.5:c.-39-160T>C	ENSP00000452724.1:n.-39-160T>C
ENST00000558566.1:c.399+204T>C	ENSP00000453025.1:n.399+204T>C
ENST00000559019.1:c.193-596T>C	ENSP00000453675.1:n.193-596T>C
ENST00000559147.1:n.410-160T>C
ENST00000559969.5:c.356-160T>C
ENST00000626689.2:c.399+204T>C	ENSP00000486681.1:n.399+204T>C
ENST00000646753.1:c.295-160T>C	ENSP00000494065.1:n.295-160T>C
ENST00000699682.1:n.703-160T>C
ENST00000699683.1:n.840-160T>C
ENST00000699684.1:c.410-160T>C	ENSP00000514523.1:n.410-160T>C
ENST00000699685.1:n.808+204T>C
ENST00000699686.1:c.193-160T>C	ENSP00000514524.1:n.193-160T>C
ENST00000699687.1:c.295-160T>C	ENSP00000514525.1:n.295-160T>C
ENST00000699688.1:n.707+204T>C
ENST00000699689.1:n.956-160T>C
ENST00000699690.1:n.906T>C
ENST00000699691.1:n.906T>C
ENST00000699693.1:n.673-160T>C
ENST00000699694.1:n.915-160T>C
ENST00000699695.1:c.294+204T>C	ENSP00000514526.1:n.294+204T>C
ENST00000699696.1:n.703-160T>C
ENST00000699697.1:c.400-160T>C	ENSP00000514527.1:n.400-160T>C
ENST00000699698.1:n.321-160T>C
ENST00000699699.1:n.493-160T>C
ENST00000699700.1:n.703-160T>C
ENST00000699701.1:c.400-160T>C	ENSP00000514528.1:n.400-160T>C
XM_005267528.2:c.400-160T>C	XP_005267585.1:n.400-160T>C
XM_005267529.2:c.295-160T>C	XP_005267586.1:n.295-160T>C
XM_011536642.1:c.400-160T>C	XP_011534944.1:n.400-160T>C
XM_011536642.2:c.400-160T>C	XP_011534944.1:n.400-160T>C
XM_017021216.2:c.-38-596T>C	XP_016876705.1:n.-38-596T>C