Canonical Allele Identifier: CA381585402
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048967T>A , CM000673.2:g.68048967T>A GRCh38
NC_000011.9:g.67816434T>A , CM000673.1:g.67816434T>A GRCh37
NC_000011.8:g.67573010T>A NCBI36
NG_007878.1:g.14952T>A , LRG_115:g.14952T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.268T>A
ENST00000698254.1:c.1172T>A ENSP00000513629.1:p.Phe391Tyr
ENST00000698255.1:c.1592T>A ENSP00000513630.1:p.Phe531Tyr
ENST00000698256.1:c.1109T>A
ENST00000698257.1:n.1061T>A
ENST00000698258.1:n.778T>A
ENST00000698259.1:n.544T>A
ENST00000265686.8:c.1643T>A MANE Select ENSP00000265686.3:p.Phe548Tyr
ENST00000265686.7:c.1643T>A ENSP00000265686.3:p.Phe548Tyr
ENST00000525724.5:n.955T>A
ENST00000532635.5:c.995T>A ENSP00000434407.1:p.Phe332Tyr
ENST00000533005.5:n.756T>A
NM_006019.3:c.1643T>A NP_006010.2:p.Phe548Tyr
NM_006053.3:c.995T>A NP_006044.1:p.Phe332Tyr
XM_005273709.2:c.1643T>A XP_005273766.1:p.Phe548Tyr
XM_011544726.1:c.1643T>A XP_011543028.1:p.Phe548Tyr
XM_011544727.1:c.1643T>A XP_011543029.1:p.Phe548Tyr
XM_011544728.1:c.1643T>A XP_011543030.1:p.Phe548Tyr
XR_949754.1:n.1647T>A
NM_001351059.1:c.749T>A NP_001337988.1:p.Phe250Tyr
XM_024448320.1:c.1736T>A XP_024304088.1:p.Phe579Tyr
XM_024448321.1:c.1736T>A XP_024304089.1:p.Phe579Tyr
XM_024448322.1:c.1736T>A XP_024304090.1:p.Phe579Tyr
XM_024448323.1:c.1736T>A XP_024304091.1:p.Phe579Tyr
XM_024448324.1:c.1736T>A XP_024304092.1:p.Phe579Tyr
XR_001747721.2:n.1767T>A
XR_001747722.1:n.1780T>A
XR_001747723.2:n.1780T>A
XR_002957115.1:n.1858T>A
NM_006019.4:c.1643T>A MANE Select NP_006010.2:p.Phe548Tyr
NM_001351059.2:c.749T>A NP_001337988.1:p.Phe250Tyr
NM_006053.4:c.995T>A NP_006044.1:p.Phe332Tyr