Canonical Allele Identifier: CA1980429679
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047770A= , CM000673.2:g.68047770A= GRCh38
NC_000011.9:g.67815237A= , CM000673.1:g.67815237A= GRCh37
NC_000011.8:g.67571813A= NCBI36
NG_007878.1:g.13755A= , LRG_115:g.13755A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.54A=
ENST00000698254.1:c.958A= ENSP00000513629.1:p.Ser320=
ENST00000698255.1:c.1378A= ENSP00000513630.1:p.Ser460=
ENST00000698256.1:c.895A=
ENST00000698257.1:n.847A=
ENST00000698258.1:n.487A=
ENST00000698259.1:n.253A=
ENST00000265686.8:c.1429A= MANE Select ENSP00000265686.3:p.Ser477=
ENST00000265686.7:c.1429A= ENSP00000265686.3:p.Ser477=
ENST00000525516.1:n.223A=
ENST00000525724.5:n.741A=
ENST00000528981.5:c.581A=
ENST00000529364.1:c.840A=
ENST00000532635.5:c.781A= ENSP00000434407.1:p.Ser261=
ENST00000533005.5:n.465A=
NM_006019.3:c.1429A= NP_006010.2:p.Ser477=
NM_006053.3:c.781A= NP_006044.1:p.Ser261=
XM_005273709.2:c.1429A= XP_005273766.1:p.Ser477=
XM_011544726.1:c.1429A= XP_011543028.1:p.Ser477=
XM_011544727.1:c.1429A= XP_011543029.1:p.Ser477=
XM_011544728.1:c.1429A= XP_011543030.1:p.Ser477=
XM_011544729.1:c.1445A= XP_011543031.1:p.Glu482=
XR_949754.1:n.1433A=
NM_001351059.1:c.535A= NP_001337988.1:p.Ser179=
XM_024448320.1:c.1445A= XP_024304088.1:p.Glu482=
XM_024448321.1:c.1445A= XP_024304089.1:p.Glu482=
XM_024448322.1:c.1445A= XP_024304090.1:p.Glu482=
XM_024448323.1:c.1445A= XP_024304091.1:p.Glu482=
XM_024448324.1:c.1445A= XP_024304092.1:p.Glu482=
XR_001747721.2:n.1553A=
XR_001747722.1:n.1566A=
XR_001747723.2:n.1566A=
XR_002957115.1:n.1567A=
NM_006019.4:c.1429A= MANE Select NP_006010.2:p.Ser477=
NM_001351059.2:c.535A= NP_001337988.1:p.Ser179=
NM_006053.4:c.781A= NP_006044.1:p.Ser261=