Canonical Allele Identifier: CA381584491
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047905C>A , CM000673.2:g.68047905C>A GRCh38
NC_000011.9:g.67815372C>A , CM000673.1:g.67815372C>A GRCh37
NC_000011.8:g.67571948C>A NCBI36
NG_007878.1:g.13890C>A , LRG_115:g.13890C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.112C>A
ENST00000698254.1:c.1016C>A ENSP00000513629.1:p.Thr339Lys
ENST00000698255.1:c.1436C>A ENSP00000513630.1:p.Thr479Lys
ENST00000698256.1:c.953C>A
ENST00000698257.1:n.905C>A
ENST00000698258.1:n.622C>A
ENST00000698259.1:n.388C>A
ENST00000265686.8:c.1487C>A MANE Select ENSP00000265686.3:p.Thr496Lys
ENST00000265686.7:c.1487C>A ENSP00000265686.3:p.Thr496Lys
ENST00000525516.1:n.281C>A
ENST00000525724.5:n.799C>A
ENST00000528981.5:c.639C>A
ENST00000532635.5:c.839C>A ENSP00000434407.1:p.Thr280Lys
ENST00000533005.5:n.600C>A
NM_006019.3:c.1487C>A NP_006010.2:p.Thr496Lys
NM_006053.3:c.839C>A NP_006044.1:p.Thr280Lys
XM_005273709.2:c.1487C>A XP_005273766.1:p.Thr496Lys
XM_011544726.1:c.1487C>A XP_011543028.1:p.Thr496Lys
XM_011544727.1:c.1487C>A XP_011543029.1:p.Thr496Lys
XM_011544728.1:c.1487C>A XP_011543030.1:p.Thr496Lys
XR_949754.1:n.1491C>A
NM_001351059.1:c.593C>A NP_001337988.1:p.Thr198Lys
XM_024448320.1:c.1580C>A XP_024304088.1:p.Thr527Lys
XM_024448321.1:c.1580C>A XP_024304089.1:p.Thr527Lys
XM_024448322.1:c.1580C>A XP_024304090.1:p.Thr527Lys
XM_024448323.1:c.1580C>A XP_024304091.1:p.Thr527Lys
XM_024448324.1:c.1580C>A XP_024304092.1:p.Thr527Lys
XR_001747721.2:n.1611C>A
XR_001747722.1:n.1624C>A
XR_001747723.2:n.1624C>A
XR_002957115.1:n.1702C>A
NM_006019.4:c.1487C>A MANE Select NP_006010.2:p.Thr496Lys
NM_001351059.2:c.593C>A NP_001337988.1:p.Thr198Lys
NM_006053.4:c.839C>A NP_006044.1:p.Thr280Lys