Canonical Allele Identifier: CA2573332451
Community Standard Title: NM_006019.4(TCIRG1):c.702del (p.Ile235SerfsTer?)
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68043642del , CM000673.2:g.68043642del GRCh38
NC_000011.9:g.67811109del , CM000673.1:g.67811109del GRCh37
NC_000011.8:g.67567685del NCBI36
NG_007878.1:g.9627del , LRG_115:g.9627del

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.702del MANE Select NP_006010.2:p.Ile235SerfsTer?
ENST00000265686.8:c.702del MANE Select ENSP00000265686.3:p.Ile235SerfsTer?
NM_001351059.1:c.-209del NP_001337988.1:n.-209del
NM_001351059.2:c.-209del NP_001337988.1:n.-209del
NM_006019.3:c.702del NP_006010.2:p.Ile235SerfsTer?
NM_006053.3:c.54del NP_006044.1:p.Ile19SerfsTer?
NM_006053.4:c.54del NP_006044.1:p.Ile19SerfsTer?
ENST00000265686.7:c.702del ENSP00000265686.3:p.Ile235SerfsTer?
ENST00000524598.5:c.660del ENSP00000432846.1:p.Ile221SerfsTer?
ENST00000527530.1:n.320del
ENST00000529364.1:c.202del
ENST00000532635.5:c.54del ENSP00000434407.1:p.Ile19SerfsTer?
ENST00000534673.5:c.*50del ENSP00000431174.1:n.*50del
ENST00000698254.1:c.404-557del ENSP00000513629.1:n.404-557del
ENST00000698255.1:c.651del ENSP00000513630.1:p.Ile218SerfsTer?
ENST00000698256.1:c.152del
ENST00000698257.1:n.120del
XM_005273709.2:c.702del XP_005273766.1:p.Ile235SerfsTer?
XM_011544726.1:c.702del XP_011543028.1:p.Ile235SerfsTer?
XM_011544727.1:c.702del XP_011543029.1:p.Ile235SerfsTer?
XM_011544728.1:c.702del XP_011543030.1:p.Ile235SerfsTer?
XM_011544729.1:c.702del XP_011543031.1:p.Ile235SerfsTer?
XM_024448320.1:c.702del XP_024304088.1:p.Ile235SerfsTer?
XM_024448321.1:c.702del XP_024304089.1:p.Ile235SerfsTer?
XM_024448322.1:c.702del XP_024304090.1:p.Ile235SerfsTer?
XM_024448323.1:c.702del XP_024304091.1:p.Ile235SerfsTer?
XM_024448324.1:c.702del XP_024304092.1:p.Ile235SerfsTer?
XR_001747721.2:n.826del
XR_001747722.1:n.823del
XR_001747723.2:n.823del
XR_002957115.1:n.824del
XR_949754.1:n.706del