Canonical Allele Identifier: CA389225423

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709828C>T (hg19) ; chr14:g.24240622C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240622C>T , CM000676.2:g.24240622C>T	GRCh38
NC_000014.8:g.24709828C>T , CM000676.1:g.24709828C>T	GRCh37
NC_000014.7:g.23779668C>T	NCBI36
NG_016650.1:g.7053G>A
NG_054634.1:g.13206C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557915.2:n.1161G>A
ENST00000557921.3:c.750G>A	ENSP00000453157.3:p.Met250Ile
ENST00000699682.1:n.1248G>A
ENST00000699683.1:n.1298G>A
ENST00000699684.1:c.*451G>A	ENSP00000514523.1:n.*451G>A
ENST00000699685.1:n.1062G>A
ENST00000699686.1:c.651G>A	ENSP00000514524.1:p.Met217Ile
ENST00000699687.1:c.753G>A	ENSP00000514525.1:p.Met251Ile
ENST00000699688.1:n.1058G>A
ENST00000699689.1:n.1414G>A
ENST00000699690.1:n.1611G>A
ENST00000699691.1:n.1755G>A
ENST00000699693.1:n.1275G>A
ENST00000699694.1:n.1517G>A
ENST00000699695.1:c.*230G>A	ENSP00000514526.1:n.*230G>A
ENST00000699696.1:n.1161G>A
ENST00000699697.1:c.858G>A	ENSP00000514527.1:p.Met286Ile
ENST00000699698.1:n.779G>A
ENST00000699699.1:n.1182G>A
ENST00000699700.1:n.1305G>A
ENST00000699701.1:c.*238G>A	ENSP00000514528.1:n.*238G>A
ENST00000267415.12:c.858G>A MANE Select	ENSP00000267415.7:p.Met286Ile
ENST00000557921.2:c.750G>A	ENSP00000453157.2:p.Met250Ile
ENST00000646753.1:c.753G>A	ENSP00000494065.1:p.Met251Ile
ENST00000267415.11:c.858G>A	ENSP00000267415.7:p.Met286Ile
ENST00000399423.8:c.858G>A	ENSP00000382350.4:p.Met286Ile
ENST00000558476.5:c.420G>A	ENSP00000452724.1:p.Met140Ile
ENST00000558566.1:c.*230G>A	ENSP00000453025.1:n.*230G>A
ENST00000559019.1:c.*230G>A	ENSP00000453675.1:n.*230G>A
ENST00000559549.1:n.584G>A
ENST00000559969.5:c.757+57G>A
ENST00000626689.2:c.*230G>A	ENSP00000486681.1:n.*230G>A
NM_001099274.1:c.858G>A	NP_001092744.1:p.Met286Ile
NM_012461.2:c.858G>A	NP_036593.2:p.Met286Ile
XM_005267528.2:c.858G>A	XP_005267585.1:p.Met286Ile
XM_005267529.2:c.753G>A	XP_005267586.1:p.Met251Ile
NM_001099274.2:c.858G>A	NP_001092744.1:p.Met286Ile
NM_001363668.1:c.753G>A	NP_001350597.1:p.Met251Ile
NM_012461.3:c.858G>A	NP_036593.2:p.Met286Ile
XM_011536642.2:c.*238G>A	XP_011534944.1:n.*238G>A
XM_017021216.2:c.216G>A	XP_016876705.1:p.Met72Ile
XM_017021217.1:c.216G>A	XP_016876706.1:p.Met72Ile
NM_001099274.3:c.858G>A MANE Select	NP_001092744.1:p.Met286Ile
NM_001363668.2:c.753G>A	NP_001350597.1:p.Met251Ile