Canonical Allele Identifier: CA2697548727

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 2759159
• ClinVar RCV Id: RCV003564590

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047921del , CM000673.2:g.68047921del	GRCh38
NC_000011.9:g.67815388del , CM000673.1:g.67815388del	GRCh37
NC_000011.8:g.67571964del	NCBI36
NG_007878.1:g.13906del , LRG_115:g.13906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.128del
ENST00000698254.1:c.1032del	ENSP00000513629.1:p.Asn346ThrfsTer25
ENST00000698255.1:c.1452del	ENSP00000513630.1:p.Asn486ThrfsTer25
ENST00000698256.1:c.969del
ENST00000698257.1:n.921del
ENST00000698258.1:n.638del
ENST00000698259.1:n.404del
ENST00000265686.8:c.1503del MANE Select	ENSP00000265686.3:p.Asn503ThrfsTer25
ENST00000265686.7:c.1503del	ENSP00000265686.3:p.Asn503ThrfsTer25
ENST00000525516.1:n.297del
ENST00000525724.5:n.815del
ENST00000528981.5:c.655del
ENST00000532635.5:c.855del	ENSP00000434407.1:p.Asn287ThrfsTer25
ENST00000533005.5:n.616del
NM_006019.3:c.1503del	NP_006010.2:p.Asn503ThrfsTer25
NM_006053.3:c.855del	NP_006044.1:p.Asn287ThrfsTer25
XM_005273709.2:c.1503del	XP_005273766.1:p.Asn503ThrfsTer25
XM_011544726.1:c.1503del	XP_011543028.1:p.Asn503ThrfsTer25
XM_011544727.1:c.1503del	XP_011543029.1:p.Asn503ThrfsTer25
XM_011544728.1:c.1503del	XP_011543030.1:p.Asn503ThrfsTer25
XR_949754.1:n.1507del
NM_001351059.1:c.609del	NP_001337988.1:p.Asn205ThrfsTer25
XM_024448320.1:c.1596del	XP_024304088.1:p.Asn534ThrfsTer25
XM_024448321.1:c.1596del	XP_024304089.1:p.Asn534ThrfsTer25
XM_024448322.1:c.1596del	XP_024304090.1:p.Asn534ThrfsTer25
XM_024448323.1:c.1596del	XP_024304091.1:p.Asn534ThrfsTer25
XM_024448324.1:c.1596del	XP_024304092.1:p.Asn534ThrfsTer25
XR_001747721.2:n.1627del
XR_001747722.1:n.1640del
XR_001747723.2:n.1640del
XR_002957115.1:n.1718del
NM_006019.4:c.1503del MANE Select	NP_006010.2:p.Asn503ThrfsTer25
NM_001351059.2:c.609del	NP_001337988.1:p.Asn205ThrfsTer25
NM_006053.4:c.855del	NP_006044.1:p.Asn287ThrfsTer25