Canonical Allele Identifier: CA10640021

Gene: TINF2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24242423G>A , CM000676.2:g.24242423G>A	GRCh38
NC_000014.8:g.24711629G>A , CM000676.1:g.24711629G>A	GRCh37
NC_000014.7:g.23781469G>A	NCBI36
NG_016650.1:g.5252C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001099274.3:c.-91C>T MANE Select	NP_001092744.1:n.-91C>T
ENST00000267415.12:c.-91C>T MANE Select	ENSP00000267415.7:n.-91C>T
NM_001099274.1:c.-91C>T	NP_001092744.1:n.-91C>T
NM_001099274.2:c.-91C>T	NP_001092744.1:n.-91C>T
NM_001363668.1:c.-91C>T	NP_001350597.1:n.-91C>T
NM_001363668.2:c.-91C>T	NP_001350597.1:n.-91C>T
NM_012461.2:c.-91C>T	NP_036593.2:n.-91C>T
NM_012461.3:c.-91C>T	NP_036593.2:n.-91C>T
ENST00000267415.11:c.-91C>T	ENSP00000267415.7:n.-91C>T
ENST00000399423.8:c.-91C>T	ENSP00000382350.4:n.-91C>T
ENST00000557915.2:n.213C>T
ENST00000557921.1:c.-91C>T	ENSP00000453157.1:n.-91C>T
ENST00000558476.5:c.-293C>T	ENSP00000452724.1:n.-293C>T
ENST00000558510.1:n.213C>T
ENST00000558566.1:c.-91C>T	ENSP00000453025.1:n.-91C>T
ENST00000559019.1:c.-91C>T	ENSP00000453675.1:n.-91C>T
ENST00000626689.2:c.-91C>T	ENSP00000486681.1:n.-91C>T
ENST00000646753.1:c.-91C>T	ENSP00000494065.1:n.-91C>T
ENST00000699682.1:n.213C>T
ENST00000699683.1:n.204C>T
ENST00000699684.1:c.-91C>T	ENSP00000514523.1:n.-91C>T
ENST00000699685.1:n.173C>T
ENST00000699687.1:c.-91C>T	ENSP00000514525.1:n.-91C>T
ENST00000699688.1:n.72C>T
ENST00000699689.1:n.207C>T
ENST00000699690.1:n.213C>T
ENST00000699691.1:n.213C>T
ENST00000699694.1:n.166C>T
ENST00000699695.1:c.-91C>T	ENSP00000514526.1:n.-91C>T
ENST00000699696.1:n.213C>T
ENST00000699697.1:c.-91C>T	ENSP00000514527.1:n.-91C>T
ENST00000699700.1:n.213C>T
ENST00000699701.1:c.-91C>T	ENSP00000514528.1:n.-91C>T
XM_005267528.2:c.-91C>T	XP_005267585.1:n.-91C>T
XM_005267529.2:c.-91C>T	XP_005267586.1:n.-91C>T
XM_011536642.1:c.-91C>T	XP_011534944.1:n.-91C>T
XM_011536642.2:c.-91C>T	XP_011534944.1:n.-91C>T
XM_017021216.2:c.-321C>T	XP_016876705.1:n.-321C>T