Canonical Allele Identifier: CA485782338

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709966A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240760A>T , CM000676.2:g.24240760A>T	GRCh38
NC_000014.8:g.24709966A>T , CM000676.1:g.24709966A>T	GRCh37
NC_000014.7:g.23779806A>T	NCBI36
NG_016650.1:g.6915T>A
NG_054634.1:g.13344A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1023T>A
ENST00000557921.3:c.612T>A	ENSP00000453157.3:p.Leu204=
ENST00000699682.1:n.1110T>A
ENST00000699683.1:n.1160T>A
ENST00000699684.1:c.*313T>A	ENSP00000514523.1:n.*313T>A
ENST00000699685.1:n.924T>A
ENST00000699686.1:c.513T>A	ENSP00000514524.1:p.Leu171=
ENST00000699687.1:c.615T>A	ENSP00000514525.1:p.Leu205=
ENST00000699688.1:n.920T>A
ENST00000699689.1:n.1276T>A
ENST00000699690.1:n.1473T>A
ENST00000699691.1:n.1617T>A
ENST00000699693.1:n.1137T>A
ENST00000699694.1:n.1379T>A
ENST00000699695.1:c.*92T>A	ENSP00000514526.1:n.*92T>A
ENST00000699696.1:n.1023T>A
ENST00000699697.1:c.720T>A	ENSP00000514527.1:p.Leu240=
ENST00000699698.1:n.641T>A
ENST00000699699.1:n.1044T>A
ENST00000699700.1:n.1167T>A
ENST00000699701.1:c.*100T>A	ENSP00000514528.1:n.*100T>A
ENST00000267415.12:c.720T>A MANE Select	ENSP00000267415.7:p.Leu240=
ENST00000557921.2:c.612T>A	ENSP00000453157.2:p.Leu204=
ENST00000646753.1:c.615T>A	ENSP00000494065.1:p.Leu205=
ENST00000267415.11:c.720T>A	ENSP00000267415.7:p.Leu240=
ENST00000399423.8:c.720T>A	ENSP00000382350.4:p.Leu240=
ENST00000558476.5:c.282T>A	ENSP00000452724.1:p.Leu94=
ENST00000558566.1:c.*92T>A	ENSP00000453025.1:n.*92T>A
ENST00000559019.1:c.*92T>A	ENSP00000453675.1:n.*92T>A
ENST00000559549.1:n.446T>A
ENST00000559969.5:c.676T>A
ENST00000626689.2:c.*92T>A	ENSP00000486681.1:n.*92T>A
NM_001099274.1:c.720T>A	NP_001092744.1:p.Leu240=
NM_012461.2:c.720T>A	NP_036593.2:p.Leu240=
XM_005267528.2:c.720T>A	XP_005267585.1:p.Leu240=
XM_005267529.2:c.615T>A	XP_005267586.1:p.Leu205=
NM_001099274.2:c.720T>A	NP_001092744.1:p.Leu240=
NM_001363668.1:c.615T>A	NP_001350597.1:p.Leu205=
NM_012461.3:c.720T>A	NP_036593.2:p.Leu240=
XM_011536642.2:c.*100T>A	XP_011534944.1:n.*100T>A
XM_017021216.2:c.78T>A	XP_016876705.1:p.Leu26=
XM_017021217.1:c.78T>A	XP_016876706.1:p.Leu26=
NM_001099274.3:c.720T>A MANE Select	NP_001092744.1:p.Leu240=
NM_001363668.2:c.615T>A	NP_001350597.1:p.Leu205=