Canonical Allele Identifier: CA381586791
Community Standard Title: NM_006019.4(TCIRG1):c.1782T>A (p.Cys594Ter)
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68049189T>A , CM000673.2:g.68049189T>A GRCh38
NC_000011.9:g.67816656T>A , CM000673.1:g.67816656T>A GRCh37
NC_000011.8:g.67573232T>A NCBI36
NG_007878.1:g.15174T>A , LRG_115:g.15174T>A

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.1782T>A MANE Select NP_006010.2:p.Cys594Ter
ENST00000265686.8:c.1782T>A MANE Select ENSP00000265686.3:p.Cys594Ter
NM_001351059.1:c.888T>A NP_001337988.1:p.Cys296Ter
NM_001351059.2:c.888T>A NP_001337988.1:p.Cys296Ter
NM_006019.3:c.1782T>A NP_006010.2:p.Cys594Ter
NM_006053.3:c.1134T>A NP_006044.1:p.Cys378Ter
NM_006053.4:c.1134T>A NP_006044.1:p.Cys378Ter
ENST00000265686.7:c.1782T>A ENSP00000265686.3:p.Cys594Ter
ENST00000524870.1:n.42T>A
ENST00000525724.5:n.1094T>A
ENST00000530449.2:n.407T>A
ENST00000532635.5:c.1134T>A ENSP00000434407.1:p.Cys378Ter
ENST00000533005.5:n.895T>A
ENST00000698254.1:c.1311T>A ENSP00000513629.1:p.Cys437Ter
ENST00000698255.1:c.1731T>A ENSP00000513630.1:p.Cys577Ter
ENST00000698256.1:c.1248T>A
ENST00000698257.1:n.1200T>A
ENST00000698258.1:n.917T>A
ENST00000698259.1:n.683T>A
XM_005273709.2:c.1782T>A XP_005273766.1:p.Cys594Ter
XM_011544726.1:c.1782T>A XP_011543028.1:p.Cys594Ter
XM_011544727.1:c.1782T>A XP_011543029.1:p.Cys594Ter
XM_011544728.1:c.1782T>A XP_011543030.1:p.Cys594Ter
XM_024448320.1:c.1875T>A XP_024304088.1:p.Cys625Ter
XM_024448321.1:c.1875T>A XP_024304089.1:p.Cys625Ter
XM_024448322.1:c.1875T>A XP_024304090.1:p.Cys625Ter
XM_024448323.1:c.1875T>A XP_024304091.1:p.Cys625Ter
XM_024448324.1:c.1875T>A XP_024304092.1:p.Cys625Ter
XR_001747721.2:n.1906T>A
XR_001747722.1:n.1919T>A
XR_001747723.2:n.1919T>A
XR_002957115.1:n.1997T>A
XR_949754.1:n.1786T>A