Canonical Allele Identifier: CA679554626
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1435240633

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047957del , CM000673.2:g.68047957del GRCh38
NC_000011.9:g.67815424del , CM000673.1:g.67815424del GRCh37
NC_000011.8:g.67572000del NCBI36
NG_007878.1:g.13942del , LRG_115:g.13942del

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.164del
ENST00000698254.1:c.1068del ENSP00000513629.1:p.Phe357LeufsTer14
ENST00000698255.1:c.1488del ENSP00000513630.1:p.Phe497LeufsTer14
ENST00000698256.1:c.1005del
ENST00000698257.1:n.957del
ENST00000698258.1:n.674del
ENST00000698259.1:n.440del
ENST00000265686.8:c.1539del MANE Select ENSP00000265686.3:p.Phe514LeufsTer14
ENST00000265686.7:c.1539del ENSP00000265686.3:p.Phe514LeufsTer14
ENST00000525516.1:n.333del
ENST00000525724.5:n.851del
ENST00000528981.5:c.691del
ENST00000532635.5:c.891del ENSP00000434407.1:p.Phe298LeufsTer14
ENST00000533005.5:n.652del
NM_006019.3:c.1539del NP_006010.2:p.Phe514LeufsTer14
NM_006053.3:c.891del NP_006044.1:p.Phe298LeufsTer14
XM_005273709.2:c.1539del XP_005273766.1:p.Phe514LeufsTer14
XM_011544726.1:c.1539del XP_011543028.1:p.Phe514LeufsTer14
XM_011544727.1:c.1539del XP_011543029.1:p.Phe514LeufsTer14
XM_011544728.1:c.1539del XP_011543030.1:p.Phe514LeufsTer14
XR_949754.1:n.1543del
NM_001351059.1:c.645del NP_001337988.1:p.Phe216LeufsTer14
XM_024448320.1:c.1632del XP_024304088.1:p.Phe545LeufsTer14
XM_024448321.1:c.1632del XP_024304089.1:p.Phe545LeufsTer14
XM_024448322.1:c.1632del XP_024304090.1:p.Phe545LeufsTer14
XM_024448323.1:c.1632del XP_024304091.1:p.Phe545LeufsTer14
XM_024448324.1:c.1632del XP_024304092.1:p.Phe545LeufsTer14
XR_001747721.2:n.1663del
XR_001747722.1:n.1676del
XR_001747723.2:n.1676del
XR_002957115.1:n.1754del
NM_006019.4:c.1539del MANE Select NP_006010.2:p.Phe514LeufsTer14
NM_001351059.2:c.645del NP_001337988.1:p.Phe216LeufsTer14
NM_006053.4:c.891del NP_006044.1:p.Phe298LeufsTer14