Canonical Allele Identifier: CA381584838
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048881T>G , CM000673.2:g.68048881T>G GRCh38
NC_000011.9:g.67816348T>G , CM000673.1:g.67816348T>G GRCh37
NC_000011.8:g.67572924T>G NCBI36
NG_007878.1:g.14866T>G , LRG_115:g.14866T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.182T>G
ENST00000698254.1:c.1086T>G ENSP00000513629.1:p.Ile362Met
ENST00000698255.1:c.1506T>G ENSP00000513630.1:p.Ile502Met
ENST00000698256.1:c.1023T>G
ENST00000698257.1:n.975T>G
ENST00000698258.1:n.692T>G
ENST00000698259.1:n.458T>G
ENST00000265686.8:c.1557T>G MANE Select ENSP00000265686.3:p.Ile519Met
ENST00000265686.7:c.1557T>G ENSP00000265686.3:p.Ile519Met
ENST00000525724.5:n.869T>G
ENST00000528981.5:c.709T>G
ENST00000532635.5:c.909T>G ENSP00000434407.1:p.Ile303Met
ENST00000533005.5:n.670T>G
NM_006019.3:c.1557T>G NP_006010.2:p.Ile519Met
NM_006053.3:c.909T>G NP_006044.1:p.Ile303Met
XM_005273709.2:c.1557T>G XP_005273766.1:p.Ile519Met
XM_011544726.1:c.1557T>G XP_011543028.1:p.Ile519Met
XM_011544727.1:c.1557T>G XP_011543029.1:p.Ile519Met
XM_011544728.1:c.1557T>G XP_011543030.1:p.Ile519Met
XR_949754.1:n.1561T>G
NM_001351059.1:c.663T>G NP_001337988.1:p.Ile221Met
XM_024448320.1:c.1650T>G XP_024304088.1:p.Ile550Met
XM_024448321.1:c.1650T>G XP_024304089.1:p.Ile550Met
XM_024448322.1:c.1650T>G XP_024304090.1:p.Ile550Met
XM_024448323.1:c.1650T>G XP_024304091.1:p.Ile550Met
XM_024448324.1:c.1650T>G XP_024304092.1:p.Ile550Met
XR_001747721.2:n.1681T>G
XR_001747722.1:n.1694T>G
XR_001747723.2:n.1694T>G
XR_002957115.1:n.1772T>G
NM_006019.4:c.1557T>G MANE Select NP_006010.2:p.Ile519Met
NM_001351059.2:c.663T>G NP_001337988.1:p.Ile221Met
NM_006053.4:c.909T>G NP_006044.1:p.Ile303Met