Canonical Allele Identifier: CA381584624
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047953A>G , CM000673.2:g.68047953A>G GRCh38
NC_000011.9:g.67815420A>G , CM000673.1:g.67815420A>G GRCh37
NC_000011.8:g.67571996A>G NCBI36
NG_007878.1:g.13938A>G , LRG_115:g.13938A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.160A>G
ENST00000698254.1:c.1064A>G ENSP00000513629.1:p.Tyr355Cys
ENST00000698255.1:c.1484A>G ENSP00000513630.1:p.Tyr495Cys
ENST00000698256.1:c.1001A>G
ENST00000698257.1:n.953A>G
ENST00000698258.1:n.670A>G
ENST00000698259.1:n.436A>G
ENST00000265686.8:c.1535A>G MANE Select ENSP00000265686.3:p.Tyr512Cys
ENST00000265686.7:c.1535A>G ENSP00000265686.3:p.Tyr512Cys
ENST00000525516.1:n.329A>G
ENST00000525724.5:n.847A>G
ENST00000528981.5:c.687A>G
ENST00000532635.5:c.887A>G ENSP00000434407.1:p.Tyr296Cys
ENST00000533005.5:n.648A>G
NM_006019.3:c.1535A>G NP_006010.2:p.Tyr512Cys
NM_006053.3:c.887A>G NP_006044.1:p.Tyr296Cys
XM_005273709.2:c.1535A>G XP_005273766.1:p.Tyr512Cys
XM_011544726.1:c.1535A>G XP_011543028.1:p.Tyr512Cys
XM_011544727.1:c.1535A>G XP_011543029.1:p.Tyr512Cys
XM_011544728.1:c.1535A>G XP_011543030.1:p.Tyr512Cys
XR_949754.1:n.1539A>G
NM_001351059.1:c.641A>G NP_001337988.1:p.Tyr214Cys
XM_024448320.1:c.1628A>G XP_024304088.1:p.Tyr543Cys
XM_024448321.1:c.1628A>G XP_024304089.1:p.Tyr543Cys
XM_024448322.1:c.1628A>G XP_024304090.1:p.Tyr543Cys
XM_024448323.1:c.1628A>G XP_024304091.1:p.Tyr543Cys
XM_024448324.1:c.1628A>G XP_024304092.1:p.Tyr543Cys
XR_001747721.2:n.1659A>G
XR_001747722.1:n.1672A>G
XR_001747723.2:n.1672A>G
XR_002957115.1:n.1750A>G
NM_006019.4:c.1535A>G MANE Select NP_006010.2:p.Tyr512Cys
NM_001351059.2:c.641A>G NP_001337988.1:p.Tyr214Cys
NM_006053.4:c.887A>G NP_006044.1:p.Tyr296Cys