Canonical Allele Identifier: CA381583998
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1385314
ClinVar RCV Id: RCV001902853
dbSNP Id: rs774863206

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047740C>A , CM000673.2:g.68047740C>A GRCh38
NC_000011.9:g.67815207C>A , CM000673.1:g.67815207C>A GRCh37
NC_000011.8:g.67571783C>A NCBI36
NG_007878.1:g.13725C>A , LRG_115:g.13725C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.24C>A
ENST00000698254.1:c.928C>A ENSP00000513629.1:p.Arg310Ser
ENST00000698255.1:c.1348C>A ENSP00000513630.1:p.Arg450Ser
ENST00000698256.1:c.865C>A
ENST00000698257.1:n.817C>A
ENST00000698258.1:n.457C>A
ENST00000698259.1:n.223C>A
ENST00000265686.8:c.1399C>A MANE Select ENSP00000265686.3:p.Arg467Ser
ENST00000265686.7:c.1399C>A ENSP00000265686.3:p.Arg467Ser
ENST00000525516.1:n.193C>A
ENST00000525724.5:n.711C>A
ENST00000528981.5:c.551C>A
ENST00000529364.1:c.810C>A
ENST00000532635.5:c.751C>A ENSP00000434407.1:p.Arg251Ser
ENST00000533005.5:n.435C>A
NM_006019.3:c.1399C>A NP_006010.2:p.Arg467Ser
NM_006053.3:c.751C>A NP_006044.1:p.Arg251Ser
XM_005273709.2:c.1399C>A XP_005273766.1:p.Arg467Ser
XM_011544726.1:c.1399C>A XP_011543028.1:p.Arg467Ser
XM_011544727.1:c.1399C>A XP_011543029.1:p.Arg467Ser
XM_011544728.1:c.1399C>A XP_011543030.1:p.Arg467Ser
XM_011544729.1:c.1415C>A XP_011543031.1:p.Ser472Ter
XR_949754.1:n.1403C>A
NM_001351059.1:c.505C>A NP_001337988.1:p.Arg169Ser
XM_024448320.1:c.1415C>A XP_024304088.1:p.Ser472Ter
XM_024448321.1:c.1415C>A XP_024304089.1:p.Ser472Ter
XM_024448322.1:c.1415C>A XP_024304090.1:p.Ser472Ter
XM_024448323.1:c.1415C>A XP_024304091.1:p.Ser472Ter
XM_024448324.1:c.1415C>A XP_024304092.1:p.Ser472Ter
XR_001747721.2:n.1523C>A
XR_001747722.1:n.1536C>A
XR_001747723.2:n.1536C>A
XR_002957115.1:n.1537C>A
NM_006019.4:c.1399C>A MANE Select NP_006010.2:p.Arg467Ser
NM_001351059.2:c.505C>A NP_001337988.1:p.Arg169Ser
NM_006053.4:c.751C>A NP_006044.1:p.Arg251Ser