Canonical Allele Identifier: CA389223127

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709534T>A (hg19) ; chr14:g.24240328T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240328T>A , CM000676.2:g.24240328T>A	GRCh38
NC_000014.8:g.24709534T>A , CM000676.1:g.24709534T>A	GRCh37
NC_000014.7:g.23779374T>A	NCBI36
NG_016650.1:g.7347A>T
NG_054634.1:g.12912T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1455A>T
ENST00000557921.3:c.*87A>T	ENSP00000453157.3:n.*87A>T
ENST00000699682.1:n.1542A>T
ENST00000699683.1:n.1592A>T
ENST00000699684.1:c.*745A>T	ENSP00000514523.1:n.*745A>T
ENST00000699685.1:n.1356A>T
ENST00000699686.1:c.*87A>T	ENSP00000514524.1:n.*87A>T
ENST00000699687.1:c.*87A>T	ENSP00000514525.1:n.*87A>T
ENST00000699688.1:n.1352A>T
ENST00000699689.1:n.1708A>T
ENST00000699690.1:n.1905A>T
ENST00000699691.1:n.2049A>T
ENST00000699692.1:n.3A>T
ENST00000699693.1:n.1481A>T
ENST00000699694.1:n.1811A>T
ENST00000699695.1:c.*436A>T	ENSP00000514526.1:n.*436A>T
ENST00000699696.1:n.1455A>T
ENST00000699697.1:c.1064A>T	ENSP00000514527.1:p.Asn355Ile
ENST00000699698.1:n.985A>T
ENST00000699699.1:n.1476A>T
ENST00000699700.1:n.1599A>T
ENST00000699701.1:c.*532A>T	ENSP00000514528.1:n.*532A>T
ENST00000267415.12:c.1064A>T MANE Select	ENSP00000267415.7:p.Asn355Ile
ENST00000646753.1:c.959A>T	ENSP00000494065.1:p.Asn320Ile
ENST00000267415.11:c.1064A>T	ENSP00000267415.7:p.Asn355Ile
ENST00000399423.8:c.*87A>T	ENSP00000382350.4:n.*87A>T
ENST00000557915.1:n.271A>T
ENST00000558566.1:c.*524A>T	ENSP00000453025.1:n.*524A>T
ENST00000559969.5:c.910A>T
ENST00000560019.5:c.59A>T	ENSP00000453113.1:p.Asn20Ile
ENST00000626689.2:c.*436A>T	ENSP00000486681.1:n.*436A>T
NM_001099274.1:c.1064A>T	NP_001092744.1:p.Asn355Ile
NM_012461.2:c.*87A>T	NP_036593.2:n.*87A>T
XM_005267528.2:c.1064A>T	XP_005267585.1:p.Asn355Ile
XM_005267529.2:c.959A>T	XP_005267586.1:p.Asn320Ile
NM_001099274.2:c.1064A>T	NP_001092744.1:p.Asn355Ile
NM_001363668.1:c.959A>T	NP_001350597.1:p.Asn320Ile
NM_012461.3:c.*87A>T	NP_036593.2:n.*87A>T
XM_011536642.2:c.*532A>T	XP_011534944.1:n.*532A>T
XM_017021216.2:c.422A>T	XP_016876705.1:p.Asn141Ile
XM_017021217.1:c.422A>T	XP_016876706.1:p.Asn141Ile
NM_001099274.3:c.1064A>T MANE Select	NP_001092744.1:p.Asn355Ile
NM_001363668.2:c.959A>T	NP_001350597.1:p.Asn320Ile