Canonical Allele Identifier: CA389223118

Gene: TINF2

Linked Data

• MyVariant Identifiers: chr14:g.24709533A>T (hg19) ; chr14:g.24240327A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24240327A>T , CM000676.2:g.24240327A>T	GRCh38
NC_000014.8:g.24709533A>T , CM000676.1:g.24709533A>T	GRCh37
NC_000014.7:g.23779373A>T	NCBI36
NG_016650.1:g.7348T>A
NG_054634.1:g.12911A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557915.2:n.1456T>A
ENST00000557921.3:c.*88T>A	ENSP00000453157.3:n.*88T>A
ENST00000699682.1:n.1543T>A
ENST00000699683.1:n.1593T>A
ENST00000699684.1:c.*746T>A	ENSP00000514523.1:n.*746T>A
ENST00000699685.1:n.1357T>A
ENST00000699686.1:c.*88T>A	ENSP00000514524.1:n.*88T>A
ENST00000699687.1:c.*88T>A	ENSP00000514525.1:n.*88T>A
ENST00000699688.1:n.1353T>A
ENST00000699689.1:n.1709T>A
ENST00000699690.1:n.1906T>A
ENST00000699691.1:n.2050T>A
ENST00000699692.1:n.4T>A
ENST00000699693.1:n.1482T>A
ENST00000699694.1:n.1812T>A
ENST00000699695.1:c.*437T>A	ENSP00000514526.1:n.*437T>A
ENST00000699696.1:n.1456T>A
ENST00000699697.1:c.1065T>A	ENSP00000514527.1:p.Asn355Lys
ENST00000699698.1:n.986T>A
ENST00000699699.1:n.1477T>A
ENST00000699700.1:n.1600T>A
ENST00000699701.1:c.*533T>A	ENSP00000514528.1:n.*533T>A
ENST00000267415.12:c.1065T>A MANE Select	ENSP00000267415.7:p.Asn355Lys
ENST00000646753.1:c.960T>A	ENSP00000494065.1:p.Asn320Lys
ENST00000267415.11:c.1065T>A	ENSP00000267415.7:p.Asn355Lys
ENST00000399423.8:c.*88T>A	ENSP00000382350.4:n.*88T>A
ENST00000557915.1:n.272T>A
ENST00000558566.1:c.*525T>A	ENSP00000453025.1:n.*525T>A
ENST00000559969.5:c.911T>A
ENST00000560019.5:c.60T>A	ENSP00000453113.1:p.Asn20Lys
ENST00000626689.2:c.*437T>A	ENSP00000486681.1:n.*437T>A
NM_001099274.1:c.1065T>A	NP_001092744.1:p.Asn355Lys
NM_012461.2:c.*88T>A	NP_036593.2:n.*88T>A
XM_005267528.2:c.1065T>A	XP_005267585.1:p.Asn355Lys
XM_005267529.2:c.960T>A	XP_005267586.1:p.Asn320Lys
NM_001099274.2:c.1065T>A	NP_001092744.1:p.Asn355Lys
NM_001363668.1:c.960T>A	NP_001350597.1:p.Asn320Lys
NM_012461.3:c.*88T>A	NP_036593.2:n.*88T>A
XM_011536642.2:c.*533T>A	XP_011534944.1:n.*533T>A
XM_017021216.2:c.423T>A	XP_016876705.1:p.Asn141Lys
XM_017021217.1:c.423T>A	XP_016876706.1:p.Asn141Lys
NM_001099274.3:c.1065T>A MANE Select	NP_001092744.1:p.Asn355Lys
NM_001363668.2:c.960T>A	NP_001350597.1:p.Asn320Lys