Canonical Allele Identifier: CA2580084641

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 1726406
• ClinVar RCV Id: RCV002310090

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68049291del , CM000673.2:g.68049291del	GRCh38
NC_000011.9:g.67816758del , CM000673.1:g.67816758del	GRCh37
NC_000011.8:g.67573334del	NCBI36
NG_007878.1:g.15276del , LRG_115:g.15276del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.509del
ENST00000698254.1:c.1413del	ENSP00000513629.1:p.Gln472ArgfsTer?
ENST00000698255.1:c.1833del	ENSP00000513630.1:p.Gln612ArgfsTer?
ENST00000698256.1:c.1350del
ENST00000698257.1:n.1302del
ENST00000698258.1:n.1019del
ENST00000698259.1:n.785del
ENST00000265686.8:c.1884del MANE Select	ENSP00000265686.3:p.Gln629ArgfsTer?
ENST00000265686.7:c.1884del	ENSP00000265686.3:p.Gln629ArgfsTer?
ENST00000524870.1:n.144del
ENST00000525724.5:n.1196del
ENST00000532635.5:c.1236del	ENSP00000434407.1:p.Gln413ArgfsTer?
ENST00000533005.5:n.997del
NM_006019.3:c.1884del	NP_006010.2:p.Gln629ArgfsTer?
NM_006053.3:c.1236del	NP_006044.1:p.Gln413ArgfsTer?
XM_005273709.2:c.1884del	XP_005273766.1:p.Gln629ArgfsTer?
XM_011544726.1:c.1884del	XP_011543028.1:p.Gln629ArgfsTer?
XM_011544727.1:c.1884del	XP_011543029.1:p.Gln629ArgfsTer?
XM_011544728.1:c.1884del	XP_011543030.1:p.Gln629ArgfsTer?
XR_949754.1:n.1888del
NM_001351059.1:c.990del	NP_001337988.1:p.Gln331ArgfsTer?
XM_024448320.1:c.1977del	XP_024304088.1:p.Gln660ArgfsTer?
XM_024448321.1:c.1977del	XP_024304089.1:p.Gln660ArgfsTer?
XM_024448322.1:c.1977del	XP_024304090.1:p.Gln660ArgfsTer?
XM_024448323.1:c.1977del	XP_024304091.1:p.Gln660ArgfsTer?
XM_024448324.1:c.1977del	XP_024304092.1:p.Gln660ArgfsTer?
XR_001747721.2:n.2008del
XR_001747722.1:n.2021del
XR_001747723.2:n.2021del
XR_002957115.1:n.2099del
NM_006019.4:c.1884del MANE Select	NP_006010.2:p.Gln629ArgfsTer?
NM_001351059.2:c.990del	NP_001337988.1:p.Gln331ArgfsTer?
NM_006053.4:c.1236del	NP_006044.1:p.Gln413ArgfsTer?