Canonical Allele Identifier: CA2573147498
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1456773
dbSNP Id: rs2134455711

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047800del , CM000673.2:g.68047800del GRCh38
NC_000011.9:g.67815267del , CM000673.1:g.67815267del GRCh37
NC_000011.8:g.67571843del NCBI36
NG_007878.1:g.13785del , LRG_115:g.13785del

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.84del
ENST00000698254.1:c.988del ENSP00000513629.1:p.Trp330GlyfsTer?
ENST00000698255.1:c.1408del ENSP00000513630.1:p.Trp470GlyfsTer?
ENST00000698256.1:c.925del
ENST00000698257.1:n.877del
ENST00000698258.1:n.517del
ENST00000698259.1:n.283del
ENST00000265686.8:c.1459del MANE Select ENSP00000265686.3:p.Trp487GlyfsTer?
ENST00000265686.7:c.1459del ENSP00000265686.3:p.Trp487GlyfsTer?
ENST00000525516.1:n.253del
ENST00000525724.5:n.771del
ENST00000528981.5:c.611del
ENST00000532635.5:c.811del ENSP00000434407.1:p.Trp271GlyfsTer?
ENST00000533005.5:n.495del
NM_006019.3:c.1459del NP_006010.2:p.Trp487GlyfsTer?
NM_006053.3:c.811del NP_006044.1:p.Trp271GlyfsTer?
XM_005273709.2:c.1459del XP_005273766.1:p.Trp487GlyfsTer?
XM_011544726.1:c.1459del XP_011543028.1:p.Trp487GlyfsTer?
XM_011544727.1:c.1459del XP_011543029.1:p.Trp487GlyfsTer?
XM_011544728.1:c.1459del XP_011543030.1:p.Trp487GlyfsTer?
XM_011544729.1:c.1475del XP_011543031.1:p.Leu492ArgfsTer?
XR_949754.1:n.1463del
NM_001351059.1:c.565del NP_001337988.1:p.Trp189GlyfsTer?
XM_024448320.1:c.1475del XP_024304088.1:p.Leu492ArgfsTer3
XM_024448321.1:c.1475del XP_024304089.1:p.Leu492ArgfsTer3
XM_024448322.1:c.1475del XP_024304090.1:p.Leu492ArgfsTer3
XM_024448323.1:c.1475del XP_024304091.1:p.Leu492ArgfsTer3
XM_024448324.1:c.1475del XP_024304092.1:p.Leu492ArgfsTer3
XR_001747721.2:n.1583del
XR_001747722.1:n.1596del
XR_001747723.2:n.1596del
XR_002957115.1:n.1597del
NM_006019.4:c.1459del MANE Select NP_006010.2:p.Trp487GlyfsTer?
NM_001351059.2:c.565del NP_001337988.1:p.Trp189GlyfsTer?
NM_006053.4:c.811del NP_006044.1:p.Trp271GlyfsTer?