Canonical Allele Identifier: CA389226450

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709911T>G (hg19) ; chr14:g.24240705T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240705T>G , CM000676.2:g.24240705T>G	GRCh38
NC_000014.8:g.24709911T>G , CM000676.1:g.24709911T>G	GRCh37
NC_000014.7:g.23779751T>G	NCBI36
NG_016650.1:g.6970A>C
NG_054634.1:g.13289T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1078A>C
ENST00000557921.3:c.667A>C	ENSP00000453157.3:p.Asn223His
ENST00000699682.1:n.1165A>C
ENST00000699683.1:n.1215A>C
ENST00000699684.1:c.*368A>C	ENSP00000514523.1:n.*368A>C
ENST00000699685.1:n.979A>C
ENST00000699686.1:c.568A>C	ENSP00000514524.1:p.Asn190His
ENST00000699687.1:c.670A>C	ENSP00000514525.1:p.Asn224His
ENST00000699688.1:n.975A>C
ENST00000699689.1:n.1331A>C
ENST00000699690.1:n.1528A>C
ENST00000699691.1:n.1672A>C
ENST00000699693.1:n.1192A>C
ENST00000699694.1:n.1434A>C
ENST00000699695.1:c.*147A>C	ENSP00000514526.1:n.*147A>C
ENST00000699696.1:n.1078A>C
ENST00000699697.1:c.775A>C	ENSP00000514527.1:p.Asn259His
ENST00000699698.1:n.696A>C
ENST00000699699.1:n.1099A>C
ENST00000699700.1:n.1222A>C
ENST00000699701.1:c.*155A>C	ENSP00000514528.1:n.*155A>C
ENST00000267415.12:c.775A>C MANE Select	ENSP00000267415.7:p.Asn259His
ENST00000557921.2:c.667A>C	ENSP00000453157.2:p.Asn223His
ENST00000646753.1:c.670A>C	ENSP00000494065.1:p.Asn224His
ENST00000267415.11:c.775A>C	ENSP00000267415.7:p.Asn259His
ENST00000399423.8:c.775A>C	ENSP00000382350.4:p.Asn259His
ENST00000558476.5:c.337A>C	ENSP00000452724.1:p.Asn113His
ENST00000558566.1:c.*147A>C	ENSP00000453025.1:n.*147A>C
ENST00000559019.1:c.*147A>C	ENSP00000453675.1:n.*147A>C
ENST00000559549.1:n.501A>C
ENST00000559969.5:c.731A>C
ENST00000626689.2:c.*147A>C	ENSP00000486681.1:n.*147A>C
NM_001099274.1:c.775A>C	NP_001092744.1:p.Asn259His
NM_012461.2:c.775A>C	NP_036593.2:p.Asn259His
XM_005267528.2:c.775A>C	XP_005267585.1:p.Asn259His
XM_005267529.2:c.670A>C	XP_005267586.1:p.Asn224His
NM_001099274.2:c.775A>C	NP_001092744.1:p.Asn259His
NM_001363668.1:c.670A>C	NP_001350597.1:p.Asn224His
NM_012461.3:c.775A>C	NP_036593.2:p.Asn259His
XM_011536642.2:c.*155A>C	XP_011534944.1:n.*155A>C
XM_017021216.2:c.133A>C	XP_016876705.1:p.Asn45His
XM_017021217.1:c.133A>C	XP_016876706.1:p.Asn45His
NM_001099274.3:c.775A>C MANE Select	NP_001092744.1:p.Asn259His
NM_001363668.2:c.670A>C	NP_001350597.1:p.Asn224His