Canonical Allele Identifier: CA485782172

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709867G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240661G>C , CM000676.2:g.24240661G>C	GRCh38
NC_000014.8:g.24709867G>C , CM000676.1:g.24709867G>C	GRCh37
NC_000014.7:g.23779707G>C	NCBI36
NG_016650.1:g.7014C>G
NG_054634.1:g.13245G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1122C>G
ENST00000557921.3:c.711C>G	ENSP00000453157.3:p.Ala237=
ENST00000699682.1:n.1209C>G
ENST00000699683.1:n.1259C>G
ENST00000699684.1:c.*412C>G	ENSP00000514523.1:n.*412C>G
ENST00000699685.1:n.1023C>G
ENST00000699686.1:c.612C>G	ENSP00000514524.1:p.Ala204=
ENST00000699687.1:c.714C>G	ENSP00000514525.1:p.Ala238=
ENST00000699688.1:n.1019C>G
ENST00000699689.1:n.1375C>G
ENST00000699690.1:n.1572C>G
ENST00000699691.1:n.1716C>G
ENST00000699693.1:n.1236C>G
ENST00000699694.1:n.1478C>G
ENST00000699695.1:c.*191C>G	ENSP00000514526.1:n.*191C>G
ENST00000699696.1:n.1122C>G
ENST00000699697.1:c.819C>G	ENSP00000514527.1:p.Ala273=
ENST00000699698.1:n.740C>G
ENST00000699699.1:n.1143C>G
ENST00000699700.1:n.1266C>G
ENST00000699701.1:c.*199C>G	ENSP00000514528.1:n.*199C>G
ENST00000267415.12:c.819C>G MANE Select	ENSP00000267415.7:p.Ala273=
ENST00000557921.2:c.711C>G	ENSP00000453157.2:p.Ala237=
ENST00000646753.1:c.714C>G	ENSP00000494065.1:p.Ala238=
ENST00000267415.11:c.819C>G	ENSP00000267415.7:p.Ala273=
ENST00000399423.8:c.819C>G	ENSP00000382350.4:p.Ala273=
ENST00000558476.5:c.381C>G	ENSP00000452724.1:p.Ala127=
ENST00000558566.1:c.*191C>G	ENSP00000453025.1:n.*191C>G
ENST00000559019.1:c.*191C>G	ENSP00000453675.1:n.*191C>G
ENST00000559549.1:n.545C>G
ENST00000559969.5:c.757+18C>G
ENST00000626689.2:c.*191C>G	ENSP00000486681.1:n.*191C>G
NM_001099274.1:c.819C>G	NP_001092744.1:p.Ala273=
NM_012461.2:c.819C>G	NP_036593.2:p.Ala273=
XM_005267528.2:c.819C>G	XP_005267585.1:p.Ala273=
XM_005267529.2:c.714C>G	XP_005267586.1:p.Ala238=
NM_001099274.2:c.819C>G	NP_001092744.1:p.Ala273=
NM_001363668.1:c.714C>G	NP_001350597.1:p.Ala238=
NM_012461.3:c.819C>G	NP_036593.2:p.Ala273=
XM_011536642.2:c.*199C>G	XP_011534944.1:n.*199C>G
XM_017021216.2:c.177C>G	XP_016876705.1:p.Ala59=
XM_017021217.1:c.177C>G	XP_016876706.1:p.Ala59=
NM_001099274.3:c.819C>G MANE Select	NP_001092744.1:p.Ala273=
NM_001363668.2:c.714C>G	NP_001350597.1:p.Ala238=