Canonical Allele Identifier: CA224203753

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043365C>A , CM000673.2:g.68043365C>A	GRCh38
NC_000011.9:g.67810832C>A , CM000673.1:g.67810832C>A	GRCh37
NC_000011.8:g.67567408C>A	NCBI36
NG_007878.1:g.9350C>A , LRG_115:g.9350C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.504-6C>A MANE Select	NP_006010.2:n.504-6C>A
ENST00000265686.8:c.504-6C>A MANE Select	ENSP00000265686.3:n.504-6C>A
NM_001351059.1:c.-413C>A	NP_001337988.1:n.-413C>A
NM_001351059.2:c.-413C>A	NP_001337988.1:n.-413C>A
NM_006019.3:c.504-6C>A	NP_006010.2:n.504-6C>A
NM_006053.3:c.-151C>A	NP_006044.1:n.-151C>A
NM_006053.4:c.-151C>A	NP_006044.1:n.-151C>A
ENST00000265686.7:c.504-6C>A	ENSP00000265686.3:n.504-6C>A
ENST00000524598.5:c.462-6C>A	ENSP00000432846.1:n.462-6C>A
ENST00000527530.1:n.43C>A
ENST00000529657.1:c.504-6C>A	ENSP00000435023.1:n.504-6C>A
ENST00000532635.5:c.-151C>A	ENSP00000434407.1:n.-151C>A
ENST00000533947.1:n.804C>A
ENST00000534673.5:c.504-206C>A	ENSP00000431174.1:n.504-206C>A
ENST00000698254.1:c.403+516C>A	ENSP00000513629.1:n.403+516C>A
ENST00000698255.1:c.504-6C>A	ENSP00000513630.1:n.504-6C>A
XM_005273709.2:c.504-6C>A	XP_005273766.1:n.504-6C>A
XM_011544726.1:c.504-6C>A	XP_011543028.1:n.504-6C>A
XM_011544727.1:c.504-6C>A	XP_011543029.1:n.504-6C>A
XM_011544728.1:c.504-6C>A	XP_011543030.1:n.504-6C>A
XM_011544729.1:c.504-6C>A	XP_011543031.1:n.504-6C>A
XM_024448320.1:c.504-6C>A	XP_024304088.1:n.504-6C>A
XM_024448321.1:c.504-6C>A	XP_024304089.1:n.504-6C>A
XM_024448322.1:c.504-6C>A	XP_024304090.1:n.504-6C>A
XM_024448323.1:c.504-6C>A	XP_024304091.1:n.504-6C>A
XM_024448324.1:c.504-6C>A	XP_024304092.1:n.504-6C>A
XR_001747721.2:n.628-6C>A
XR_001747722.1:n.625-6C>A
XR_001747723.2:n.625-6C>A
XR_002957115.1:n.626-6C>A
XR_949754.1:n.508-6C>A