Canonical Allele Identifier: CA389222830

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709511G>C (hg19) ; chr14:g.24240305G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240305G>C , CM000676.2:g.24240305G>C	GRCh38
NC_000014.8:g.24709511G>C , CM000676.1:g.24709511G>C	GRCh37
NC_000014.7:g.23779351G>C	NCBI36
NG_016650.1:g.7370C>G
NG_054634.1:g.12889G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1478C>G
ENST00000557921.3:c.*110C>G	ENSP00000453157.3:n.*110C>G
ENST00000699682.1:n.1565C>G
ENST00000699683.1:n.1615C>G
ENST00000699684.1:c.*768C>G	ENSP00000514523.1:n.*768C>G
ENST00000699685.1:n.1379C>G
ENST00000699686.1:c.*110C>G	ENSP00000514524.1:n.*110C>G
ENST00000699687.1:c.*110C>G	ENSP00000514525.1:n.*110C>G
ENST00000699688.1:n.1375C>G
ENST00000699689.1:n.1731C>G
ENST00000699690.1:n.1928C>G
ENST00000699691.1:n.2072C>G
ENST00000699692.1:n.26C>G
ENST00000699693.1:n.1504C>G
ENST00000699694.1:n.1834C>G
ENST00000699695.1:c.*459C>G	ENSP00000514526.1:n.*459C>G
ENST00000699696.1:n.1478C>G
ENST00000699697.1:c.1087C>G	ENSP00000514527.1:p.Pro363Ala
ENST00000699698.1:n.1008C>G
ENST00000699699.1:n.1499C>G
ENST00000699700.1:n.1622C>G
ENST00000699701.1:c.*555C>G	ENSP00000514528.1:n.*555C>G
ENST00000267415.12:c.1087C>G MANE Select	ENSP00000267415.7:p.Pro363Ala
ENST00000646753.1:c.982C>G	ENSP00000494065.1:p.Pro328Ala
ENST00000267415.11:c.1087C>G	ENSP00000267415.7:p.Pro363Ala
ENST00000399423.8:c.*110C>G	ENSP00000382350.4:n.*110C>G
ENST00000557915.1:n.294C>G
ENST00000558566.1:c.*547C>G	ENSP00000453025.1:n.*547C>G
ENST00000559969.5:c.933C>G
ENST00000560019.5:c.82C>G	ENSP00000453113.1:p.Pro28Ala
ENST00000626689.2:c.*459C>G	ENSP00000486681.1:n.*459C>G
NM_001099274.1:c.1087C>G	NP_001092744.1:p.Pro363Ala
NM_012461.2:c.*110C>G	NP_036593.2:n.*110C>G
XM_005267528.2:c.1087C>G	XP_005267585.1:p.Pro363Ala
XM_005267529.2:c.982C>G	XP_005267586.1:p.Pro328Ala
NM_001099274.2:c.1087C>G	NP_001092744.1:p.Pro363Ala
NM_001363668.1:c.982C>G	NP_001350597.1:p.Pro328Ala
NM_012461.3:c.*110C>G	NP_036593.2:n.*110C>G
XM_011536642.2:c.*555C>G	XP_011534944.1:n.*555C>G
XM_017021216.2:c.445C>G	XP_016876705.1:p.Pro149Ala
XM_017021217.1:c.445C>G	XP_016876706.1:p.Pro149Ala
NM_001099274.3:c.1087C>G MANE Select	NP_001092744.1:p.Pro363Ala
NM_001363668.2:c.982C>G	NP_001350597.1:p.Pro328Ala