Canonical Allele Identifier: CA381577131

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043390G>T , CM000673.2:g.68043390G>T	GRCh38
NC_000011.9:g.67810857G>T , CM000673.1:g.67810857G>T	GRCh37
NC_000011.8:g.67567433G>T	NCBI36
NG_007878.1:g.9375G>T , LRG_115:g.9375G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.523G>T MANE Select	NP_006010.2:p.Glu175Ter
ENST00000265686.8:c.523G>T MANE Select	ENSP00000265686.3:p.Glu175Ter
NM_001351059.1:c.-388G>T	NP_001337988.1:n.-388G>T
NM_001351059.2:c.-388G>T	NP_001337988.1:n.-388G>T
NM_006019.3:c.523G>T	NP_006010.2:p.Glu175Ter
NM_006053.3:c.-126G>T	NP_006044.1:n.-126G>T
NM_006053.4:c.-126G>T	NP_006044.1:n.-126G>T
ENST00000265686.7:c.523G>T	ENSP00000265686.3:p.Glu175Ter
ENST00000524598.5:c.481G>T	ENSP00000432846.1:p.Glu161Ter
ENST00000527530.1:n.68G>T
ENST00000529364.1:c.23G>T
ENST00000529657.1:c.523G>T	ENSP00000435023.1:p.Glu175Ter
ENST00000532635.5:c.-126G>T	ENSP00000434407.1:n.-126G>T
ENST00000533947.1:n.829G>T
ENST00000534673.5:c.504-181G>T	ENSP00000431174.1:n.504-181G>T
ENST00000698254.1:c.403+541G>T	ENSP00000513629.1:n.403+541G>T
ENST00000698255.1:c.523G>T	ENSP00000513630.1:p.Glu175Ter
XM_005273709.2:c.523G>T	XP_005273766.1:p.Glu175Ter
XM_011544726.1:c.523G>T	XP_011543028.1:p.Glu175Ter
XM_011544727.1:c.523G>T	XP_011543029.1:p.Glu175Ter
XM_011544728.1:c.523G>T	XP_011543030.1:p.Glu175Ter
XM_011544729.1:c.523G>T	XP_011543031.1:p.Glu175Ter
XM_024448320.1:c.523G>T	XP_024304088.1:p.Glu175Ter
XM_024448321.1:c.523G>T	XP_024304089.1:p.Glu175Ter
XM_024448322.1:c.523G>T	XP_024304090.1:p.Glu175Ter
XM_024448323.1:c.523G>T	XP_024304091.1:p.Glu175Ter
XM_024448324.1:c.523G>T	XP_024304092.1:p.Glu175Ter
XR_001747721.2:n.647G>T
XR_001747722.1:n.644G>T
XR_001747723.2:n.644G>T
XR_002957115.1:n.645G>T
XR_949754.1:n.527G>T