Canonical Allele Identifier: CA1980430233
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047971_68047973delinsCTG , CM000673.2:g.68047971_68047973delinsCTG GRCh38
NC_000011.9:g.67815438_67815440delinsCTG , CM000673.1:g.67815438_67815440delinsCTG GRCh37
NC_000011.8:g.67572014_67572016delinsCTG NCBI36
NG_007878.1:g.13956_13958delinsCTG , LRG_115:g.13956_13958delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.178_179+1delinsCTG
ENST00000698254.1:c.1082_1083+1delinsCTG
ENST00000698255.1:c.1502_1503+1delinsCTG
ENST00000698256.1:c.1019_1020+1delinsCTG
ENST00000698257.1:n.971_972+1delinsCTG
ENST00000698258.1:n.688_689+1delinsCTG
ENST00000698259.1:n.454_455+1delinsCTG
ENST00000265686.8:c.1553_1554+1delinsCTG
ENST00000265686.7:c.1553_1554+1delinsCTG
ENST00000525516.1:n.347_349delinsCTG
ENST00000525724.5:n.865_866+1delinsCTG
ENST00000528981.5:c.705_706+1delinsCTG
ENST00000532635.5:c.905_906+1delinsCTG
ENST00000533005.5:n.666_667+1delinsCTG
NM_006019.3:c.1553_1554+1delinsCTG
NM_006053.3:c.905_906+1delinsCTG
XM_005273709.2:c.1553_1554+1delinsCTG
XM_011544726.1:c.1553_1554+1delinsCTG
XM_011544727.1:c.1553_1554+1delinsCTG
XM_011544728.1:c.1553_1554+1delinsCTG
XR_949754.1:n.1557_1558+1delinsCTG
NM_001351059.1:c.659_660+1delinsCTG
XM_024448320.1:c.1646_1647+1delinsCTG
XM_024448321.1:c.1646_1647+1delinsCTG
XM_024448322.1:c.1646_1647+1delinsCTG
XM_024448323.1:c.1646_1647+1delinsCTG
XM_024448324.1:c.1646_1647+1delinsCTG
XR_001747721.2:n.1677_1678+1delinsCTG
XR_001747722.1:n.1690_1691+1delinsCTG
XR_001747723.2:n.1690_1691+1delinsCTG
XR_002957115.1:n.1768_1769+1delinsCTG
NM_006019.4:c.1553_1554+1delinsCTG
NM_001351059.2:c.659_660+1delinsCTG
NM_006053.4:c.905_906+1delinsCTG