Canonical Allele Identifier: CA939090432
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1855594676

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047974_68047975del , CM000673.2:g.68047974_68047975del GRCh38
NC_000011.9:g.67815441_67815442del , CM000673.1:g.67815441_67815442del GRCh37
NC_000011.8:g.67572017_67572018del NCBI36
NG_007878.1:g.13959_13960del , LRG_115:g.13959_13960del

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.179+2_179+3del
ENST00000698254.1:c.1083+2_1083+3del
ENST00000698255.1:c.1503+2_1503+3del
ENST00000698256.1:c.1020+2_1020+3del
ENST00000698257.1:n.972+2_972+3del
ENST00000698258.1:n.689+2_689+3del
ENST00000698259.1:n.455+2_455+3del
ENST00000265686.8:c.1554+2_1554+3del
ENST00000265686.7:c.1554+2_1554+3del
ENST00000525516.1:n.350_351del
ENST00000525724.5:n.866+2_866+3del
ENST00000528981.5:c.706+2_706+3del
ENST00000532635.5:c.906+2_906+3del
ENST00000533005.5:n.667+2_667+3del
NM_006019.3:c.1554+2_1554+3del
NM_006053.3:c.906+2_906+3del
XM_005273709.2:c.1554+2_1554+3del
XM_011544726.1:c.1554+2_1554+3del
XM_011544727.1:c.1554+2_1554+3del
XM_011544728.1:c.1554+2_1554+3del
XR_949754.1:n.1558+2_1558+3del
NM_001351059.1:c.660+2_660+3del
XM_024448320.1:c.1647+2_1647+3del
XM_024448321.1:c.1647+2_1647+3del
XM_024448322.1:c.1647+2_1647+3del
XM_024448323.1:c.1647+2_1647+3del
XM_024448324.1:c.1647+2_1647+3del
XR_001747721.2:n.1678+2_1678+3del
XR_001747722.1:n.1691+2_1691+3del
XR_001747723.2:n.1691+2_1691+3del
XR_002957115.1:n.1769+2_1769+3del
NM_006019.4:c.1554+2_1554+3del
NM_001351059.2:c.660+2_660+3del
NM_006053.4:c.906+2_906+3del