Canonical Allele Identifier: CA1980429773
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047790C= , CM000673.2:g.68047790C= GRCh38
NC_000011.9:g.67815257C= , CM000673.1:g.67815257C= GRCh37
NC_000011.8:g.67571833C= NCBI36
NG_007878.1:g.13775C= , LRG_115:g.13775C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.74C=
ENST00000698254.1:c.978C= ENSP00000513629.1:p.Asn326=
ENST00000698255.1:c.1398C= ENSP00000513630.1:p.Asn466=
ENST00000698256.1:c.915C=
ENST00000698257.1:n.867C=
ENST00000698258.1:n.507C=
ENST00000698259.1:n.273C=
ENST00000265686.8:c.1449C= MANE Select ENSP00000265686.3:p.Asn483=
ENST00000265686.7:c.1449C= ENSP00000265686.3:p.Asn483=
ENST00000525516.1:n.243C=
ENST00000525724.5:n.761C=
ENST00000528981.5:c.601C=
ENST00000529364.1:c.860C=
ENST00000532635.5:c.801C= ENSP00000434407.1:p.Asn267=
ENST00000533005.5:n.485C=
NM_006019.3:c.1449C= NP_006010.2:p.Asn483=
NM_006053.3:c.801C= NP_006044.1:p.Asn267=
XM_005273709.2:c.1449C= XP_005273766.1:p.Asn483=
XM_011544726.1:c.1449C= XP_011543028.1:p.Asn483=
XM_011544727.1:c.1449C= XP_011543029.1:p.Asn483=
XM_011544728.1:c.1449C= XP_011543030.1:p.Asn483=
XM_011544729.1:c.1465C= XP_011543031.1:p.Pro489=
XR_949754.1:n.1453C=
NM_001351059.1:c.555C= NP_001337988.1:p.Asn185=
XM_024448320.1:c.1465C= XP_024304088.1:p.Pro489=
XM_024448321.1:c.1465C= XP_024304089.1:p.Pro489=
XM_024448322.1:c.1465C= XP_024304090.1:p.Pro489=
XM_024448323.1:c.1465C= XP_024304091.1:p.Pro489=
XM_024448324.1:c.1465C= XP_024304092.1:p.Pro489=
XR_001747721.2:n.1573C=
XR_001747722.1:n.1586C=
XR_001747723.2:n.1586C=
XR_002957115.1:n.1587C=
NM_006019.4:c.1449C= MANE Select NP_006010.2:p.Asn483=
NM_001351059.2:c.555C= NP_001337988.1:p.Asn185=
NM_006053.4:c.801C= NP_006044.1:p.Asn267=