Canonical Allele Identifier: CA485782144

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709852G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240646G>A , CM000676.2:g.24240646G>A	GRCh38
NC_000014.8:g.24709852G>A , CM000676.1:g.24709852G>A	GRCh37
NC_000014.7:g.23779692G>A	NCBI36
NG_016650.1:g.7029C>T
NG_054634.1:g.13230G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1137C>T
ENST00000557921.3:c.726C>T	ENSP00000453157.3:p.Gly242=
ENST00000699682.1:n.1224C>T
ENST00000699683.1:n.1274C>T
ENST00000699684.1:c.*427C>T	ENSP00000514523.1:n.*427C>T
ENST00000699685.1:n.1038C>T
ENST00000699686.1:c.627C>T	ENSP00000514524.1:p.Gly209=
ENST00000699687.1:c.729C>T	ENSP00000514525.1:p.Gly243=
ENST00000699688.1:n.1034C>T
ENST00000699689.1:n.1390C>T
ENST00000699690.1:n.1587C>T
ENST00000699691.1:n.1731C>T
ENST00000699693.1:n.1251C>T
ENST00000699694.1:n.1493C>T
ENST00000699695.1:c.*206C>T	ENSP00000514526.1:n.*206C>T
ENST00000699696.1:n.1137C>T
ENST00000699697.1:c.834C>T	ENSP00000514527.1:p.Gly278=
ENST00000699698.1:n.755C>T
ENST00000699699.1:n.1158C>T
ENST00000699700.1:n.1281C>T
ENST00000699701.1:c.*214C>T	ENSP00000514528.1:n.*214C>T
ENST00000267415.12:c.834C>T MANE Select	ENSP00000267415.7:p.Gly278=
ENST00000557921.2:c.726C>T	ENSP00000453157.2:p.Gly242=
ENST00000646753.1:c.729C>T	ENSP00000494065.1:p.Gly243=
ENST00000267415.11:c.834C>T	ENSP00000267415.7:p.Gly278=
ENST00000399423.8:c.834C>T	ENSP00000382350.4:p.Gly278=
ENST00000558476.5:c.396C>T	ENSP00000452724.1:p.Gly132=
ENST00000558566.1:c.*206C>T	ENSP00000453025.1:n.*206C>T
ENST00000559019.1:c.*206C>T	ENSP00000453675.1:n.*206C>T
ENST00000559549.1:n.560C>T
ENST00000559969.5:c.757+33C>T
ENST00000626689.2:c.*206C>T	ENSP00000486681.1:n.*206C>T
NM_001099274.1:c.834C>T	NP_001092744.1:p.Gly278=
NM_012461.2:c.834C>T	NP_036593.2:p.Gly278=
XM_005267528.2:c.834C>T	XP_005267585.1:p.Gly278=
XM_005267529.2:c.729C>T	XP_005267586.1:p.Gly243=
NM_001099274.2:c.834C>T	NP_001092744.1:p.Gly278=
NM_001363668.1:c.729C>T	NP_001350597.1:p.Gly243=
NM_012461.3:c.834C>T	NP_036593.2:p.Gly278=
XM_011536642.2:c.*214C>T	XP_011534944.1:n.*214C>T
XM_017021216.2:c.192C>T	XP_016876705.1:p.Gly64=
XM_017021217.1:c.192C>T	XP_016876706.1:p.Gly64=
NM_001099274.3:c.834C>T MANE Select	NP_001092744.1:p.Gly278=
NM_001363668.2:c.729C>T	NP_001350597.1:p.Gly243=