Canonical Allele Identifier: CA389223155

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709535T>G (hg19) ; chr14:g.24240329T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240329T>G , CM000676.2:g.24240329T>G	GRCh38
NC_000014.8:g.24709535T>G , CM000676.1:g.24709535T>G	GRCh37
NC_000014.7:g.23779375T>G	NCBI36
NG_016650.1:g.7346A>C
NG_054634.1:g.12913T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1454A>C
ENST00000557921.3:c.*86A>C	ENSP00000453157.3:n.*86A>C
ENST00000699682.1:n.1541A>C
ENST00000699683.1:n.1591A>C
ENST00000699684.1:c.*744A>C	ENSP00000514523.1:n.*744A>C
ENST00000699685.1:n.1355A>C
ENST00000699686.1:c.*86A>C	ENSP00000514524.1:n.*86A>C
ENST00000699687.1:c.*86A>C	ENSP00000514525.1:n.*86A>C
ENST00000699688.1:n.1351A>C
ENST00000699689.1:n.1707A>C
ENST00000699690.1:n.1904A>C
ENST00000699691.1:n.2048A>C
ENST00000699692.1:n.2A>C
ENST00000699693.1:n.1480A>C
ENST00000699694.1:n.1810A>C
ENST00000699695.1:c.*435A>C	ENSP00000514526.1:n.*435A>C
ENST00000699696.1:n.1454A>C
ENST00000699697.1:c.1063A>C	ENSP00000514527.1:p.Asn355His
ENST00000699698.1:n.984A>C
ENST00000699699.1:n.1475A>C
ENST00000699700.1:n.1598A>C
ENST00000699701.1:c.*531A>C	ENSP00000514528.1:n.*531A>C
ENST00000267415.12:c.1063A>C MANE Select	ENSP00000267415.7:p.Asn355His
ENST00000646753.1:c.958A>C	ENSP00000494065.1:p.Asn320His
ENST00000267415.11:c.1063A>C	ENSP00000267415.7:p.Asn355His
ENST00000399423.8:c.*86A>C	ENSP00000382350.4:n.*86A>C
ENST00000557915.1:n.270A>C
ENST00000558566.1:c.*523A>C	ENSP00000453025.1:n.*523A>C
ENST00000559969.5:c.909A>C
ENST00000560019.5:c.58A>C	ENSP00000453113.1:p.Asn20His
ENST00000626689.2:c.*435A>C	ENSP00000486681.1:n.*435A>C
NM_001099274.1:c.1063A>C	NP_001092744.1:p.Asn355His
NM_012461.2:c.*86A>C	NP_036593.2:n.*86A>C
XM_005267528.2:c.1063A>C	XP_005267585.1:p.Asn355His
XM_005267529.2:c.958A>C	XP_005267586.1:p.Asn320His
NM_001099274.2:c.1063A>C	NP_001092744.1:p.Asn355His
NM_001363668.1:c.958A>C	NP_001350597.1:p.Asn320His
NM_012461.3:c.*86A>C	NP_036593.2:n.*86A>C
XM_011536642.2:c.*531A>C	XP_011534944.1:n.*531A>C
XM_017021216.2:c.421A>C	XP_016876705.1:p.Asn141His
XM_017021217.1:c.421A>C	XP_016876706.1:p.Asn141His
NM_001099274.3:c.1063A>C MANE Select	NP_001092744.1:p.Asn355His
NM_001363668.2:c.958A>C	NP_001350597.1:p.Asn320His