Canonical Allele Identifier: CA381576947

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043015C>T , CM000673.2:g.68043015C>T	GRCh38
NC_000011.9:g.67810482C>T , CM000673.1:g.67810482C>T	GRCh37
NC_000011.8:g.67567058C>T	NCBI36
NG_007878.1:g.9000C>T , LRG_115:g.9000C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.487C>T MANE Select	NP_006010.2:p.Gln163Ter
ENST00000265686.8:c.487C>T MANE Select	ENSP00000265686.3:p.Gln163Ter
NM_001351059.1:c.-763C>T	NP_001337988.1:n.-763C>T
NM_001351059.2:c.-763C>T	NP_001337988.1:n.-763C>T
NM_006019.3:c.487C>T	NP_006010.2:p.Gln163Ter
NM_006053.3:c.-501C>T	NP_006044.1:n.-501C>T
NM_006053.4:c.-501C>T	NP_006044.1:n.-501C>T
ENST00000265686.7:c.487C>T	ENSP00000265686.3:p.Gln163Ter
ENST00000524598.5:c.445C>T	ENSP00000432846.1:p.Gln149Ter
ENST00000529657.1:c.487C>T	ENSP00000435023.1:p.Gln163Ter
ENST00000532635.5:c.-501C>T	ENSP00000434407.1:n.-501C>T
ENST00000533947.1:n.454C>T
ENST00000534673.5:c.487C>T	ENSP00000431174.1:p.Gln163Ter
ENST00000698254.1:c.403+166C>T	ENSP00000513629.1:n.403+166C>T
ENST00000698255.1:c.487C>T	ENSP00000513630.1:p.Gln163Ter
XM_005273709.2:c.487C>T	XP_005273766.1:p.Gln163Ter
XM_011544726.1:c.487C>T	XP_011543028.1:p.Gln163Ter
XM_011544727.1:c.487C>T	XP_011543029.1:p.Gln163Ter
XM_011544728.1:c.487C>T	XP_011543030.1:p.Gln163Ter
XM_011544729.1:c.487C>T	XP_011543031.1:p.Gln163Ter
XM_024448320.1:c.487C>T	XP_024304088.1:p.Gln163Ter
XM_024448321.1:c.487C>T	XP_024304089.1:p.Gln163Ter
XM_024448322.1:c.487C>T	XP_024304090.1:p.Gln163Ter
XM_024448323.1:c.487C>T	XP_024304091.1:p.Gln163Ter
XM_024448324.1:c.487C>T	XP_024304092.1:p.Gln163Ter
XR_001747721.2:n.611C>T
XR_001747722.1:n.608C>T
XR_001747723.2:n.608C>T
XR_002957115.1:n.609C>T
XR_949754.1:n.491C>T