Canonical Allele Identifier: CA1139662063

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68042925A>G , CM000673.2:g.68042925A>G	GRCh38
NC_000011.9:g.67810392A>G , CM000673.1:g.67810392A>G	GRCh37
NC_000011.8:g.67566968A>G	NCBI36
NG_007878.1:g.8910A>G , LRG_115:g.8910A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.418-21A>G MANE Select	NP_006010.2:n.418-21A>G
ENST00000265686.8:c.418-21A>G MANE Select	ENSP00000265686.3:n.418-21A>G
NM_001351059.1:c.-832-21A>G	NP_001337988.1:n.-832-21A>G
NM_001351059.2:c.-832-21A>G	NP_001337988.1:n.-832-21A>G
NM_006019.3:c.418-21A>G	NP_006010.2:n.418-21A>G
ENST00000265686.7:c.418-21A>G	ENSP00000265686.3:n.418-21A>G
ENST00000524598.5:c.376-21A>G	ENSP00000432846.1:n.376-21A>G
ENST00000529657.1:c.418-21A>G	ENSP00000435023.1:n.418-21A>G
ENST00000533947.1:n.385-21A>G
ENST00000534673.5:c.418-21A>G	ENSP00000431174.1:n.418-21A>G
ENST00000698254.1:c.403+76A>G	ENSP00000513629.1:n.403+76A>G
ENST00000698255.1:c.418-21A>G	ENSP00000513630.1:n.418-21A>G
XM_005273709.2:c.418-21A>G	XP_005273766.1:n.418-21A>G
XM_011544726.1:c.418-21A>G	XP_011543028.1:n.418-21A>G
XM_011544727.1:c.418-21A>G	XP_011543029.1:n.418-21A>G
XM_011544728.1:c.418-21A>G	XP_011543030.1:n.418-21A>G
XM_011544729.1:c.418-21A>G	XP_011543031.1:n.418-21A>G
XM_024448320.1:c.418-21A>G	XP_024304088.1:n.418-21A>G
XM_024448321.1:c.418-21A>G	XP_024304089.1:n.418-21A>G
XM_024448322.1:c.418-21A>G	XP_024304090.1:n.418-21A>G
XM_024448323.1:c.418-21A>G	XP_024304091.1:n.418-21A>G
XM_024448324.1:c.418-21A>G	XP_024304092.1:n.418-21A>G
XR_001747721.2:n.542-21A>G
XR_001747722.1:n.539-21A>G
XR_001747723.2:n.539-21A>G
XR_002957115.1:n.540-21A>G
XR_949754.1:n.422-21A>G