Canonical Allele Identifier: CA389225921

Gene: TINF2

Linked Data

• dbSNP Id: rs1228329506
• gnomAD v3: 14-24240662-G-T
• gnomAD v4: 14-24240662-G-T
• MyVariant Identifiers: chr14:g.24709868G>T (hg19) ; chr14:g.24240662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240662G>T , CM000676.2:g.24240662G>T	GRCh38
NC_000014.8:g.24709868G>T , CM000676.1:g.24709868G>T	GRCh37
NC_000014.7:g.23779708G>T	NCBI36
NG_016650.1:g.7013C>A
NG_054634.1:g.13246G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1121C>A
ENST00000557921.3:c.710C>A	ENSP00000453157.3:p.Ala237Asp
ENST00000699682.1:n.1208C>A
ENST00000699683.1:n.1258C>A
ENST00000699684.1:c.*411C>A	ENSP00000514523.1:n.*411C>A
ENST00000699685.1:n.1022C>A
ENST00000699686.1:c.611C>A	ENSP00000514524.1:p.Ala204Asp
ENST00000699687.1:c.713C>A	ENSP00000514525.1:p.Ala238Asp
ENST00000699688.1:n.1018C>A
ENST00000699689.1:n.1374C>A
ENST00000699690.1:n.1571C>A
ENST00000699691.1:n.1715C>A
ENST00000699693.1:n.1235C>A
ENST00000699694.1:n.1477C>A
ENST00000699695.1:c.*190C>A	ENSP00000514526.1:n.*190C>A
ENST00000699696.1:n.1121C>A
ENST00000699697.1:c.818C>A	ENSP00000514527.1:p.Ala273Asp
ENST00000699698.1:n.739C>A
ENST00000699699.1:n.1142C>A
ENST00000699700.1:n.1265C>A
ENST00000699701.1:c.*198C>A	ENSP00000514528.1:n.*198C>A
ENST00000267415.12:c.818C>A MANE Select	ENSP00000267415.7:p.Ala273Asp
ENST00000557921.2:c.710C>A	ENSP00000453157.2:p.Ala237Asp
ENST00000646753.1:c.713C>A	ENSP00000494065.1:p.Ala238Asp
ENST00000267415.11:c.818C>A	ENSP00000267415.7:p.Ala273Asp
ENST00000399423.8:c.818C>A	ENSP00000382350.4:p.Ala273Asp
ENST00000558476.5:c.380C>A	ENSP00000452724.1:p.Ala127Asp
ENST00000558566.1:c.*190C>A	ENSP00000453025.1:n.*190C>A
ENST00000559019.1:c.*190C>A	ENSP00000453675.1:n.*190C>A
ENST00000559549.1:n.544C>A
ENST00000559969.5:c.757+17C>A
ENST00000626689.2:c.*190C>A	ENSP00000486681.1:n.*190C>A
NM_001099274.1:c.818C>A	NP_001092744.1:p.Ala273Asp
NM_012461.2:c.818C>A	NP_036593.2:p.Ala273Asp
XM_005267528.2:c.818C>A	XP_005267585.1:p.Ala273Asp
XM_005267529.2:c.713C>A	XP_005267586.1:p.Ala238Asp
NM_001099274.2:c.818C>A	NP_001092744.1:p.Ala273Asp
NM_001363668.1:c.713C>A	NP_001350597.1:p.Ala238Asp
NM_012461.3:c.818C>A	NP_036593.2:p.Ala273Asp
XM_011536642.2:c.*198C>A	XP_011534944.1:n.*198C>A
XM_017021216.2:c.176C>A	XP_016876705.1:p.Ala59Asp
XM_017021217.1:c.176C>A	XP_016876706.1:p.Ala59Asp
NM_001099274.3:c.818C>A MANE Select	NP_001092744.1:p.Ala273Asp
NM_001363668.2:c.713C>A	NP_001350597.1:p.Ala238Asp