Canonical Allele Identifier: CA2614700619

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68048020-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048025del , CM000673.2:g.68048025del	GRCh38
NC_000011.9:g.67815492del , CM000673.1:g.67815492del	GRCh37
NC_000011.8:g.67572068del	NCBI36
NG_007878.1:g.14010del , LRG_115:g.14010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.179+53del
ENST00000698254.1:c.1083+53del	ENSP00000513629.1:n.1083+53del
ENST00000698255.1:c.1503+53del	ENSP00000513630.1:n.1503+53del
ENST00000698256.1:c.1020+53del
ENST00000698257.1:n.972+53del
ENST00000698258.1:n.689+53del
ENST00000698259.1:n.455+53del
ENST00000265686.8:c.1554+53del MANE Select	ENSP00000265686.3:n.1554+53del
ENST00000265686.7:c.1554+53del	ENSP00000265686.3:n.1554+53del
ENST00000525516.1:n.401del
ENST00000525724.5:n.866+53del
ENST00000528981.5:c.706+53del
ENST00000532635.5:c.906+53del	ENSP00000434407.1:n.906+53del
ENST00000533005.5:n.667+53del
NM_006019.3:c.1554+53del	NP_006010.2:n.1554+53del
NM_006053.3:c.906+53del	NP_006044.1:n.906+53del
XM_005273709.2:c.1554+53del	XP_005273766.1:n.1554+53del
XM_011544726.1:c.1554+53del	XP_011543028.1:n.1554+53del
XM_011544727.1:c.1554+53del	XP_011543029.1:n.1554+53del
XM_011544728.1:c.1554+53del	XP_011543030.1:n.1554+53del
XR_949754.1:n.1558+53del
NM_001351059.1:c.660+53del	NP_001337988.1:n.660+53del
XM_024448320.1:c.1647+53del	XP_024304088.1:n.1647+53del
XM_024448321.1:c.1647+53del	XP_024304089.1:n.1647+53del
XM_024448322.1:c.1647+53del	XP_024304090.1:n.1647+53del
XM_024448323.1:c.1647+53del	XP_024304091.1:n.1647+53del
XM_024448324.1:c.1647+53del	XP_024304092.1:n.1647+53del
XR_001747721.2:n.1678+53del
XR_001747722.1:n.1691+53del
XR_001747723.2:n.1691+53del
XR_002957115.1:n.1769+53del
NM_006019.4:c.1554+53del MANE Select	NP_006010.2:n.1554+53del
NM_001351059.2:c.660+53del	NP_001337988.1:n.660+53del
NM_006053.4:c.906+53del	NP_006044.1:n.906+53del