Canonical Allele Identifier: CA1980457434
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68039747C= , CM000673.2:g.68039747C= GRCh38
NC_000011.9:g.67807214C= , CM000673.1:g.67807214C= GRCh37
NC_000011.8:g.67563790C= NCBI36
NG_007878.1:g.5732C= , LRG_115:g.5732C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.-5+628C= ENSP00000513629.1:n.-5+628C=
ENST00000698255.1:c.-5+628C= ENSP00000513630.1:n.-5+628C=
ENST00000265686.8:c.-5+628C= MANE Select ENSP00000265686.3:n.-5+628C=
ENST00000265686.7:c.-5+628C= ENSP00000265686.3:n.-5+628C=
ENST00000524598.5:c.-5+628C= ENSP00000432846.1:n.-5+628C=
ENST00000529657.1:c.-175-45C= ENSP00000435023.1:n.-175-45C=
ENST00000533947.1:n.5+628C=
ENST00000534673.5:c.-5+628C= ENSP00000431174.1:n.-5+628C=
NM_006019.3:c.-5+628C= NP_006010.2:n.-5+628C=
XM_005273709.2:c.-175-45C= XP_005273766.1:n.-175-45C=
NM_001351059.1:c.-1254+628C= NP_001337988.1:n.-1254+628C=
XM_024448320.1:c.-5+628C= XP_024304088.1:n.-5+628C=
XM_024448321.1:c.-175-45C= XP_024304089.1:n.-175-45C=
XM_024448323.1:c.-5+628C= XP_024304091.1:n.-5+628C=
XM_024448324.1:c.-5+628C= XP_024304092.1:n.-5+628C=
XR_001747721.2:n.120+628C=
XR_001747722.1:n.117+628C=
XR_001747723.2:n.117+628C=
XR_002957115.1:n.118+628C=
NM_006019.4:c.-5+628C= MANE Select NP_006010.2:n.-5+628C=
NM_001351059.2:c.-1254+628C= NP_001337988.1:n.-1254+628C=