Canonical Allele Identifier: CA600238438
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1339346552

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047683del , CM000673.2:g.68047683del GRCh38
NC_000011.9:g.67815150del , CM000673.1:g.67815150del GRCh37
NC_000011.8:g.67571726del NCBI36
NG_007878.1:g.13668del , LRG_115:g.13668del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.871del ENSP00000513629.1:p.Leu291CysfsTer?
ENST00000698255.1:c.1291del ENSP00000513630.1:p.Leu431CysfsTer?
ENST00000698256.1:c.808del
ENST00000698257.1:n.760del
ENST00000698258.1:n.400del
ENST00000698259.1:n.166del
ENST00000265686.8:c.1342del MANE Select ENSP00000265686.3:p.Leu448CysfsTer?
ENST00000265686.7:c.1342del ENSP00000265686.3:p.Leu448CysfsTer?
ENST00000525516.1:n.136del
ENST00000525724.5:n.654del
ENST00000528981.5:c.494del
ENST00000529364.1:c.753del
ENST00000532635.5:c.694del ENSP00000434407.1:p.Leu232CysfsTer?
ENST00000533005.5:n.378del
NM_006019.3:c.1342del NP_006010.2:p.Leu448CysfsTer?
NM_006053.3:c.694del NP_006044.1:p.Leu232CysfsTer?
XM_005273709.2:c.1342del XP_005273766.1:p.Leu448CysfsTer?
XM_011544726.1:c.1342del XP_011543028.1:p.Leu448CysfsTer?
XM_011544727.1:c.1342del XP_011543029.1:p.Leu448CysfsTer?
XM_011544728.1:c.1342del XP_011543030.1:p.Leu448CysfsTer?
XM_011544729.1:c.1358del XP_011543031.1:p.Pro453LeufsTer?
XR_949754.1:n.1346del
NM_001351059.1:c.448del NP_001337988.1:p.Leu150CysfsTer?
XM_024448320.1:c.1358del XP_024304088.1:p.Pro453LeufsTer?
XM_024448321.1:c.1358del XP_024304089.1:p.Pro453LeufsTer?
XM_024448322.1:c.1358del XP_024304090.1:p.Pro453LeufsTer?
XM_024448323.1:c.1358del XP_024304091.1:p.Pro453LeufsTer?
XM_024448324.1:c.1358del XP_024304092.1:p.Pro453LeufsTer?
XR_001747721.2:n.1466del
XR_001747722.1:n.1479del
XR_001747723.2:n.1479del
XR_002957115.1:n.1480del
NM_006019.4:c.1342del MANE Select NP_006010.2:p.Leu448CysfsTer?
NM_001351059.2:c.448del NP_001337988.1:p.Leu150CysfsTer?
NM_006053.4:c.694del NP_006044.1:p.Leu232CysfsTer?