Canonical Allele Identifier: CA2614700369
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047828del , CM000673.2:g.68047828del GRCh38
NC_000011.9:g.67815295del , CM000673.1:g.67815295del GRCh37
NC_000011.8:g.67571871del NCBI36
NG_007878.1:g.13813del , LRG_115:g.13813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.88+24del
ENST00000698254.1:c.992+24del ENSP00000513629.1:n.992+24del
ENST00000698255.1:c.1412+24del ENSP00000513630.1:n.1412+24del
ENST00000698256.1:c.929+24del
ENST00000698257.1:n.881+24del
ENST00000698258.1:n.545del
ENST00000698259.1:n.311del
ENST00000265686.8:c.1463+24del MANE Select ENSP00000265686.3:n.1463+24del
ENST00000265686.7:c.1463+24del ENSP00000265686.3:n.1463+24del
ENST00000525516.1:n.257+24del
ENST00000525724.5:n.775+24del
ENST00000528981.5:c.615+24del
ENST00000532635.5:c.815+24del ENSP00000434407.1:n.815+24del
ENST00000533005.5:n.523del
NM_006019.3:c.1463+24del NP_006010.2:n.1463+24del
NM_006053.3:c.815+24del NP_006044.1:n.815+24del
XM_005273709.2:c.1463+24del XP_005273766.1:n.1463+24del
XM_011544726.1:c.1463+24del XP_011543028.1:n.1463+24del
XM_011544727.1:c.1463+24del XP_011543029.1:n.1463+24del
XM_011544728.1:c.1463+24del XP_011543030.1:n.1463+24del
XM_011544729.1:c.1479+24del XP_011543031.1:n.1479+24del
XR_949754.1:n.1467+24del
NM_001351059.1:c.569+24del NP_001337988.1:n.569+24del
XM_024448320.1:c.1503del XP_024304088.1:p.Trp502GlyfsTer?
XM_024448321.1:c.1503del XP_024304089.1:p.Trp502GlyfsTer?
XM_024448322.1:c.1503del XP_024304090.1:p.Trp502GlyfsTer?
XM_024448323.1:c.1503del XP_024304091.1:p.Trp502GlyfsTer?
XM_024448324.1:c.1503del XP_024304092.1:p.Trp502GlyfsTer?
XR_001747721.2:n.1587+24del
XR_001747722.1:n.1600+24del
XR_001747723.2:n.1600+24del
XR_002957115.1:n.1625del
NM_006019.4:c.1463+24del MANE Select NP_006010.2:n.1463+24del
NM_001351059.2:c.569+24del NP_001337988.1:n.569+24del
NM_006053.4:c.815+24del NP_006044.1:n.815+24del