Canonical Allele Identifier: CA389223918

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709695G>A (hg19) ; chr14:g.24240489G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240489G>A , CM000676.2:g.24240489G>A	GRCh38
NC_000014.8:g.24709695G>A , CM000676.1:g.24709695G>A	GRCh37
NC_000014.7:g.23779535G>A	NCBI36
NG_016650.1:g.7186C>T
NG_054634.1:g.13073G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1294C>T
ENST00000557921.3:c.883C>T	ENSP00000453157.3:p.Pro295Ser
ENST00000699682.1:n.1381C>T
ENST00000699683.1:n.1431C>T
ENST00000699684.1:c.*584C>T	ENSP00000514523.1:n.*584C>T
ENST00000699685.1:n.1195C>T
ENST00000699686.1:c.784C>T	ENSP00000514524.1:p.Pro262Ser
ENST00000699687.1:c.886C>T	ENSP00000514525.1:p.Pro296Ser
ENST00000699688.1:n.1191C>T
ENST00000699689.1:n.1547C>T
ENST00000699690.1:n.1744C>T
ENST00000699691.1:n.1888C>T
ENST00000699693.1:n.1408C>T
ENST00000699694.1:n.1650C>T
ENST00000699695.1:c.*363C>T	ENSP00000514526.1:n.*363C>T
ENST00000699696.1:n.1294C>T
ENST00000699697.1:c.991C>T	ENSP00000514527.1:p.Pro331Ser
ENST00000699698.1:n.912C>T
ENST00000699699.1:n.1315C>T
ENST00000699700.1:n.1438C>T
ENST00000699701.1:c.*371C>T	ENSP00000514528.1:n.*371C>T
ENST00000267415.12:c.991C>T MANE Select	ENSP00000267415.7:p.Pro331Ser
ENST00000646753.1:c.886C>T	ENSP00000494065.1:p.Pro296Ser
ENST00000267415.11:c.991C>T	ENSP00000267415.7:p.Pro331Ser
ENST00000399423.8:c.991C>T	ENSP00000382350.4:p.Pro331Ser
ENST00000557915.1:n.110C>T
ENST00000558566.1:c.*363C>T	ENSP00000453025.1:n.*363C>T
ENST00000559019.1:c.*363C>T	ENSP00000453675.1:n.*363C>T
ENST00000559969.5:c.758-9C>T
ENST00000626689.2:c.*363C>T	ENSP00000486681.1:n.*363C>T
NM_001099274.1:c.991C>T	NP_001092744.1:p.Pro331Ser
NM_012461.2:c.991C>T	NP_036593.2:p.Pro331Ser
XM_005267528.2:c.991C>T	XP_005267585.1:p.Pro331Ser
XM_005267529.2:c.886C>T	XP_005267586.1:p.Pro296Ser
NM_001099274.2:c.991C>T	NP_001092744.1:p.Pro331Ser
NM_001363668.1:c.886C>T	NP_001350597.1:p.Pro296Ser
NM_012461.3:c.991C>T	NP_036593.2:p.Pro331Ser
XM_011536642.2:c.*371C>T	XP_011534944.1:n.*371C>T
XM_017021216.2:c.349C>T	XP_016876705.1:p.Pro117Ser
XM_017021217.1:c.349C>T	XP_016876706.1:p.Pro117Ser
NM_001099274.3:c.991C>T MANE Select	NP_001092744.1:p.Pro331Ser
NM_001363668.2:c.886C>T	NP_001350597.1:p.Pro296Ser