Canonical Allele Identifier: CA6147158
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs775657670

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.178del
ENST00000698254.1:c.1082del ENSP00000513629.1:p.Pro361LeufsTer10
ENST00000698255.1:c.1502del ENSP00000513630.1:p.Pro501LeufsTer10
ENST00000698256.1:c.1019del
ENST00000698257.1:n.971del
ENST00000698258.1:n.688del
ENST00000698259.1:n.454del
ENST00000265686.8:c.1553del MANE Select ENSP00000265686.3:p.Pro518LeufsTer10
ENST00000265686.7:c.1553del ENSP00000265686.3:p.Pro518LeufsTer10
ENST00000525516.1:n.347del
ENST00000525724.5:n.865del
ENST00000528981.5:c.705del
ENST00000532635.5:c.905del ENSP00000434407.1:p.Pro302LeufsTer10
ENST00000533005.5:n.666del
NM_006019.3:c.1553del NP_006010.2:p.Pro518LeufsTer10
NM_006053.3:c.905del NP_006044.1:p.Pro302LeufsTer10
XM_005273709.2:c.1553del XP_005273766.1:p.Pro518LeufsTer10
XM_011544726.1:c.1553del XP_011543028.1:p.Pro518LeufsTer10
XM_011544727.1:c.1553del XP_011543029.1:p.Pro518LeufsTer10
XM_011544728.1:c.1553del XP_011543030.1:p.Pro518LeufsTer10
XR_949754.1:n.1557del
NM_001351059.1:c.659del NP_001337988.1:p.Pro220LeufsTer10
XM_024448320.1:c.1646del XP_024304088.1:p.Pro549LeufsTer10
XM_024448321.1:c.1646del XP_024304089.1:p.Pro549LeufsTer10
XM_024448322.1:c.1646del XP_024304090.1:p.Pro549LeufsTer10
XM_024448323.1:c.1646del XP_024304091.1:p.Pro549LeufsTer10
XM_024448324.1:c.1646del XP_024304092.1:p.Pro549LeufsTer10
XR_001747721.2:n.1677del
XR_001747722.1:n.1690del
XR_001747723.2:n.1690del
XR_002957115.1:n.1768del
NM_006019.4:c.1553del MANE Select NP_006010.2:p.Pro518LeufsTer10
NM_001351059.2:c.659del NP_001337988.1:p.Pro220LeufsTer10
NM_006053.4:c.905del NP_006044.1:p.Pro302LeufsTer10