Canonical Allele Identifier: CA1980429766
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047789A= , CM000673.2:g.68047789A= GRCh38
NC_000011.9:g.67815256A= , CM000673.1:g.67815256A= GRCh37
NC_000011.8:g.67571832A= NCBI36
NG_007878.1:g.13774A= , LRG_115:g.13774A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.73A=
ENST00000698254.1:c.977A= ENSP00000513629.1:p.Asn326=
ENST00000698255.1:c.1397A= ENSP00000513630.1:p.Asn466=
ENST00000698256.1:c.914A=
ENST00000698257.1:n.866A=
ENST00000698258.1:n.506A=
ENST00000698259.1:n.272A=
ENST00000265686.8:c.1448A= MANE Select ENSP00000265686.3:p.Asn483=
ENST00000265686.7:c.1448A= ENSP00000265686.3:p.Asn483=
ENST00000525516.1:n.242A=
ENST00000525724.5:n.760A=
ENST00000528981.5:c.600A=
ENST00000529364.1:c.859A=
ENST00000532635.5:c.800A= ENSP00000434407.1:p.Asn267=
ENST00000533005.5:n.484A=
NM_006019.3:c.1448A= NP_006010.2:p.Asn483=
NM_006053.3:c.800A= NP_006044.1:p.Asn267=
XM_005273709.2:c.1448A= XP_005273766.1:p.Asn483=
XM_011544726.1:c.1448A= XP_011543028.1:p.Asn483=
XM_011544727.1:c.1448A= XP_011543029.1:p.Asn483=
XM_011544728.1:c.1448A= XP_011543030.1:p.Asn483=
XM_011544729.1:c.1464A= XP_011543031.1:p.Gln488=
XR_949754.1:n.1452A=
NM_001351059.1:c.554A= NP_001337988.1:p.Asn185=
XM_024448320.1:c.1464A= XP_024304088.1:p.Gln488=
XM_024448321.1:c.1464A= XP_024304089.1:p.Gln488=
XM_024448322.1:c.1464A= XP_024304090.1:p.Gln488=
XM_024448323.1:c.1464A= XP_024304091.1:p.Gln488=
XM_024448324.1:c.1464A= XP_024304092.1:p.Gln488=
XR_001747721.2:n.1572A=
XR_001747722.1:n.1585A=
XR_001747723.2:n.1585A=
XR_002957115.1:n.1586A=
NM_006019.4:c.1448A= MANE Select NP_006010.2:p.Asn483=
NM_001351059.2:c.554A= NP_001337988.1:p.Asn185=
NM_006053.4:c.800A= NP_006044.1:p.Asn267=