Canonical Allele Identifier: CA381584877
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048886G>T , CM000673.2:g.68048886G>T GRCh38
NC_000011.9:g.67816353G>T , CM000673.1:g.67816353G>T GRCh37
NC_000011.8:g.67572929G>T NCBI36
NG_007878.1:g.14871G>T , LRG_115:g.14871G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.187G>T
ENST00000698254.1:c.1091G>T ENSP00000513629.1:p.Ser364Ile
ENST00000698255.1:c.1511G>T ENSP00000513630.1:p.Ser504Ile
ENST00000698256.1:c.1028G>T
ENST00000698257.1:n.980G>T
ENST00000698258.1:n.697G>T
ENST00000698259.1:n.463G>T
ENST00000265686.8:c.1562G>T MANE Select ENSP00000265686.3:p.Ser521Ile
ENST00000265686.7:c.1562G>T ENSP00000265686.3:p.Ser521Ile
ENST00000525724.5:n.874G>T
ENST00000528981.5:c.714G>T
ENST00000532635.5:c.914G>T ENSP00000434407.1:p.Ser305Ile
ENST00000533005.5:n.675G>T
NM_006019.3:c.1562G>T NP_006010.2:p.Ser521Ile
NM_006053.3:c.914G>T NP_006044.1:p.Ser305Ile
XM_005273709.2:c.1562G>T XP_005273766.1:p.Ser521Ile
XM_011544726.1:c.1562G>T XP_011543028.1:p.Ser521Ile
XM_011544727.1:c.1562G>T XP_011543029.1:p.Ser521Ile
XM_011544728.1:c.1562G>T XP_011543030.1:p.Ser521Ile
XR_949754.1:n.1566G>T
NM_001351059.1:c.668G>T NP_001337988.1:p.Ser223Ile
XM_024448320.1:c.1655G>T XP_024304088.1:p.Ser552Ile
XM_024448321.1:c.1655G>T XP_024304089.1:p.Ser552Ile
XM_024448322.1:c.1655G>T XP_024304090.1:p.Ser552Ile
XM_024448323.1:c.1655G>T XP_024304091.1:p.Ser552Ile
XM_024448324.1:c.1655G>T XP_024304092.1:p.Ser552Ile
XR_001747721.2:n.1686G>T
XR_001747722.1:n.1699G>T
XR_001747723.2:n.1699G>T
XR_002957115.1:n.1777G>T
NM_006019.4:c.1562G>T MANE Select NP_006010.2:p.Ser521Ile
NM_001351059.2:c.668G>T NP_001337988.1:p.Ser223Ile
NM_006053.4:c.914G>T NP_006044.1:p.Ser305Ile