Canonical Allele Identifier: CA1980430173
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047954C= , CM000673.2:g.68047954C= GRCh38
NC_000011.9:g.67815421C= , CM000673.1:g.67815421C= GRCh37
NC_000011.8:g.67571997C= NCBI36
NG_007878.1:g.13939C= , LRG_115:g.13939C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.161C=
ENST00000698254.1:c.1065C= ENSP00000513629.1:p.Tyr355=
ENST00000698255.1:c.1485C= ENSP00000513630.1:p.Tyr495=
ENST00000698256.1:c.1002C=
ENST00000698257.1:n.954C=
ENST00000698258.1:n.671C=
ENST00000698259.1:n.437C=
ENST00000265686.8:c.1536C= MANE Select ENSP00000265686.3:p.Tyr512=
ENST00000265686.7:c.1536C= ENSP00000265686.3:p.Tyr512=
ENST00000525516.1:n.330C=
ENST00000525724.5:n.848C=
ENST00000528981.5:c.688C=
ENST00000532635.5:c.888C= ENSP00000434407.1:p.Tyr296=
ENST00000533005.5:n.649C=
NM_006019.3:c.1536C= NP_006010.2:p.Tyr512=
NM_006053.3:c.888C= NP_006044.1:p.Tyr296=
XM_005273709.2:c.1536C= XP_005273766.1:p.Tyr512=
XM_011544726.1:c.1536C= XP_011543028.1:p.Tyr512=
XM_011544727.1:c.1536C= XP_011543029.1:p.Tyr512=
XM_011544728.1:c.1536C= XP_011543030.1:p.Tyr512=
XR_949754.1:n.1540C=
NM_001351059.1:c.642C= NP_001337988.1:p.Tyr214=
XM_024448320.1:c.1629C= XP_024304088.1:p.Tyr543=
XM_024448321.1:c.1629C= XP_024304089.1:p.Tyr543=
XM_024448322.1:c.1629C= XP_024304090.1:p.Tyr543=
XM_024448323.1:c.1629C= XP_024304091.1:p.Tyr543=
XM_024448324.1:c.1629C= XP_024304092.1:p.Tyr543=
XR_001747721.2:n.1660C=
XR_001747722.1:n.1673C=
XR_001747723.2:n.1673C=
XR_002957115.1:n.1751C=
NM_006019.4:c.1536C= MANE Select NP_006010.2:p.Tyr512=
NM_001351059.2:c.642C= NP_001337988.1:p.Tyr214=
NM_006053.4:c.888C= NP_006044.1:p.Tyr296=