Canonical Allele Identifier: CA224208506
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2918899
ClinVar RCV Id: RCV003739191
dbSNP Id: rs376554417

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047871C>T , CM000673.2:g.68047871C>T GRCh38
NC_000011.9:g.67815338C>T , CM000673.1:g.67815338C>T GRCh37
NC_000011.8:g.67571914C>T NCBI36
NG_007878.1:g.13856C>T , LRG_115:g.13856C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.89-11C>T
ENST00000698254.1:c.993-11C>T ENSP00000513629.1:n.993-11C>T
ENST00000698255.1:c.1413-11C>T ENSP00000513630.1:n.1413-11C>T
ENST00000698256.1:c.930-11C>T
ENST00000698257.1:n.882-11C>T
ENST00000698258.1:n.588C>T
ENST00000698259.1:n.354C>T
ENST00000265686.8:c.1464-11C>T MANE Select ENSP00000265686.3:n.1464-11C>T
ENST00000265686.7:c.1464-11C>T ENSP00000265686.3:n.1464-11C>T
ENST00000525516.1:n.258-11C>T
ENST00000525724.5:n.776-11C>T
ENST00000528981.5:c.616-11C>T
ENST00000532635.5:c.816-11C>T ENSP00000434407.1:n.816-11C>T
ENST00000533005.5:n.566C>T
NM_006019.3:c.1464-11C>T NP_006010.2:n.1464-11C>T
NM_006053.3:c.816-11C>T NP_006044.1:n.816-11C>T
XM_005273709.2:c.1464-11C>T XP_005273766.1:n.1464-11C>T
XM_011544726.1:c.1464-11C>T XP_011543028.1:n.1464-11C>T
XM_011544727.1:c.1464-11C>T XP_011543029.1:n.1464-11C>T
XM_011544728.1:c.1464-11C>T XP_011543030.1:n.1464-11C>T
XM_011544729.1:c.1480-11C>T XP_011543031.1:n.1480-11C>T
XR_949754.1:n.1468-11C>T
NM_001351059.1:c.570-11C>T NP_001337988.1:n.570-11C>T
XM_024448320.1:c.1546C>T XP_024304088.1:p.Arg516Cys
XM_024448321.1:c.1546C>T XP_024304089.1:p.Arg516Cys
XM_024448322.1:c.1546C>T XP_024304090.1:p.Arg516Cys
XM_024448323.1:c.1546C>T XP_024304091.1:p.Arg516Cys
XM_024448324.1:c.1546C>T XP_024304092.1:p.Arg516Cys
XR_001747721.2:n.1588-11C>T
XR_001747722.1:n.1601-11C>T
XR_001747723.2:n.1601-11C>T
XR_002957115.1:n.1668C>T
NM_006019.4:c.1464-11C>T MANE Select NP_006010.2:n.1464-11C>T
NM_001351059.2:c.570-11C>T NP_001337988.1:n.570-11C>T
NM_006053.4:c.816-11C>T NP_006044.1:n.816-11C>T