Canonical Allele Identifier: CA2614700628

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68048025-G-GCCCCAGCCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048026_68048027insCCCAGCCCCCAC , CM000673.2:g.68048026_68048027insCCCAGCCCCCAC	GRCh38
NC_000011.9:g.67815493_67815494insCCCAGCCCCCAC , CM000673.1:g.67815493_67815494insCCCAGCCCCCAC	GRCh37
NC_000011.8:g.67572069_67572070insCCCAGCCCCCAC	NCBI36
NG_007878.1:g.14011_14012insCCCAGCCCCCAC , LRG_115:g.14011_14012insCCCAGCCCCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.179+54_179+55insCCCAGCCCCCAC
ENST00000698254.1:c.1083+54_1083+55insCCCAGCCCCCAC	ENSP00000513629.1:n.1083+54_1083+55insCCCAGCCCCCAC
ENST00000698255.1:c.1503+54_1503+55insCCCAGCCCCCAC	ENSP00000513630.1:n.1503+54_1503+55insCCCAGCCCCCAC
ENST00000698256.1:c.1020+54_1020+55insCCCAGCCCCCAC
ENST00000698257.1:n.972+54_972+55insCCCAGCCCCCAC
ENST00000698258.1:n.689+54_689+55insCCCAGCCCCCAC
ENST00000698259.1:n.455+54_455+55insCCCAGCCCCCAC
ENST00000265686.8:c.1554+54_1554+55insCCCAGCCCCCAC MANE Select	ENSP00000265686.3:n.1554+54_1554+55insCCCAGCCCCCAC
ENST00000265686.7:c.1554+54_1554+55insCCCAGCCCCCAC	ENSP00000265686.3:n.1554+54_1554+55insCCCAGCCCCCAC
ENST00000525516.1:n.402_403insCCCAGCCCCCAC
ENST00000525724.5:n.866+54_866+55insCCCAGCCCCCAC
ENST00000528981.5:c.706+54_706+55insCCCAGCCCCCAC
ENST00000532635.5:c.906+54_906+55insCCCAGCCCCCAC	ENSP00000434407.1:n.906+54_906+55insCCCAGCCCCCAC
ENST00000533005.5:n.667+54_667+55insCCCAGCCCCCAC
NM_006019.3:c.1554+54_1554+55insCCCAGCCCCCAC	NP_006010.2:n.1554+54_1554+55insCCCAGCCCCCAC
NM_006053.3:c.906+54_906+55insCCCAGCCCCCAC	NP_006044.1:n.906+54_906+55insCCCAGCCCCCAC
XM_005273709.2:c.1554+54_1554+55insCCCAGCCCCCAC	XP_005273766.1:n.1554+54_1554+55insCCCAGCCCCCAC
XM_011544726.1:c.1554+54_1554+55insCCCAGCCCCCAC	XP_011543028.1:n.1554+54_1554+55insCCCAGCCCCCAC
XM_011544727.1:c.1554+54_1554+55insCCCAGCCCCCAC	XP_011543029.1:n.1554+54_1554+55insCCCAGCCCCCAC
XM_011544728.1:c.1554+54_1554+55insCCCAGCCCCCAC	XP_011543030.1:n.1554+54_1554+55insCCCAGCCCCCAC
XR_949754.1:n.1558+54_1558+55insCCCAGCCCCCAC
NM_001351059.1:c.660+54_660+55insCCCAGCCCCCAC	NP_001337988.1:n.660+54_660+55insCCCAGCCCCCAC
XM_024448320.1:c.1647+54_1647+55insCCCAGCCCCCAC	XP_024304088.1:n.1647+54_1647+55insCCCAGCCCCCAC
XM_024448321.1:c.1647+54_1647+55insCCCAGCCCCCAC	XP_024304089.1:n.1647+54_1647+55insCCCAGCCCCCAC
XM_024448322.1:c.1647+54_1647+55insCCCAGCCCCCAC	XP_024304090.1:n.1647+54_1647+55insCCCAGCCCCCAC
XM_024448323.1:c.1647+54_1647+55insCCCAGCCCCCAC	XP_024304091.1:n.1647+54_1647+55insCCCAGCCCCCAC
XM_024448324.1:c.1647+54_1647+55insCCCAGCCCCCAC	XP_024304092.1:n.1647+54_1647+55insCCCAGCCCCCAC
XR_001747721.2:n.1678+54_1678+55insCCCAGCCCCCAC
XR_001747722.1:n.1691+54_1691+55insCCCAGCCCCCAC
XR_001747723.2:n.1691+54_1691+55insCCCAGCCCCCAC
XR_002957115.1:n.1769+54_1769+55insCCCAGCCCCCAC
NM_006019.4:c.1554+54_1554+55insCCCAGCCCCCAC MANE Select	NP_006010.2:n.1554+54_1554+55insCCCAGCCCCCAC
NM_001351059.2:c.660+54_660+55insCCCAGCCCCCAC	NP_001337988.1:n.660+54_660+55insCCCAGCCCCCAC
NM_006053.4:c.906+54_906+55insCCCAGCCCCCAC	NP_006044.1:n.906+54_906+55insCCCAGCCCCCAC