Canonical Allele Identifier: CA381577019

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043032G>A , CM000673.2:g.68043032G>A	GRCh38
NC_000011.9:g.67810499G>A , CM000673.1:g.67810499G>A	GRCh37
NC_000011.8:g.67567075G>A	NCBI36
NG_007878.1:g.9017G>A , LRG_115:g.9017G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.503+1G>A MANE Select	NP_006010.2:n.503+1G>A
ENST00000265686.8:c.503+1G>A MANE Select	ENSP00000265686.3:n.503+1G>A
NM_001351059.1:c.-746G>A	NP_001337988.1:n.-746G>A
NM_001351059.2:c.-746G>A	NP_001337988.1:n.-746G>A
NM_006019.3:c.503+1G>A	NP_006010.2:n.503+1G>A
NM_006053.3:c.-484G>A	NP_006044.1:n.-484G>A
NM_006053.4:c.-484G>A	NP_006044.1:n.-484G>A
ENST00000265686.7:c.503+1G>A	ENSP00000265686.3:n.503+1G>A
ENST00000524598.5:c.461+1G>A	ENSP00000432846.1:n.461+1G>A
ENST00000529657.1:c.503+1G>A	ENSP00000435023.1:n.503+1G>A
ENST00000532635.5:c.-484G>A	ENSP00000434407.1:n.-484G>A
ENST00000533947.1:n.471G>A
ENST00000534673.5:c.503+1G>A	ENSP00000431174.1:n.503+1G>A
ENST00000698254.1:c.403+183G>A	ENSP00000513629.1:n.403+183G>A
ENST00000698255.1:c.503+1G>A	ENSP00000513630.1:n.503+1G>A
XM_005273709.2:c.503+1G>A	XP_005273766.1:n.503+1G>A
XM_011544726.1:c.503+1G>A	XP_011543028.1:n.503+1G>A
XM_011544727.1:c.503+1G>A	XP_011543029.1:n.503+1G>A
XM_011544728.1:c.503+1G>A	XP_011543030.1:n.503+1G>A
XM_011544729.1:c.503+1G>A	XP_011543031.1:n.503+1G>A
XM_024448320.1:c.503+1G>A	XP_024304088.1:n.503+1G>A
XM_024448321.1:c.503+1G>A	XP_024304089.1:n.503+1G>A
XM_024448322.1:c.503+1G>A	XP_024304090.1:n.503+1G>A
XM_024448323.1:c.503+1G>A	XP_024304091.1:n.503+1G>A
XM_024448324.1:c.503+1G>A	XP_024304092.1:n.503+1G>A
XR_001747721.2:n.627+1G>A
XR_001747722.1:n.624+1G>A
XR_001747723.2:n.624+1G>A
XR_002957115.1:n.625+1G>A
XR_949754.1:n.507+1G>A