Canonical Allele Identifier: CA2614699769

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047680-C-CGGCCTTATTCCAGAGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047680_68047681insGGCCTTATTCCAGAGGGGG , CM000673.2:g.68047680_68047681insGGCCTTATTCCAGAGGGGG	GRCh38
NC_000011.9:g.67815147_67815148insGGCCTTATTCCAGAGGGGG , CM000673.1:g.67815147_67815148insGGCCTTATTCCAGAGGGGG	GRCh37
NC_000011.8:g.67571723_67571724insGGCCTTATTCCAGAGGGGG	NCBI36
NG_007878.1:g.13665_13666insGGCCTTATTCCAGAGGGGG , LRG_115:g.13665_13666insGGCCTTATTCCAGAGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.868_869insGGCCTTATTCCAGAGGGGG	ENSP00000513629.1:p.Leu290ArgfsTer?
ENST00000698255.1:c.1288_1289insGGCCTTATTCCAGAGGGGG	ENSP00000513630.1:p.Leu430ArgfsTer?
ENST00000698256.1:c.805_806insGGCCTTATTCCAGAGGGGG
ENST00000698257.1:n.757_758insGGCCTTATTCCAGAGGGGG
ENST00000698258.1:n.397_398insGGCCTTATTCCAGAGGGGG
ENST00000698259.1:n.163_164insGGCCTTATTCCAGAGGGGG
ENST00000265686.8:c.1339_1340insGGCCTTATTCCAGAGGGGG MANE Select	ENSP00000265686.3:p.Leu447ArgfsTer?
ENST00000265686.7:c.1339_1340insGGCCTTATTCCAGAGGGGG	ENSP00000265686.3:p.Leu447ArgfsTer?
ENST00000525516.1:n.133_134insGGCCTTATTCCAGAGGGGG
ENST00000525724.5:n.651_652insGGCCTTATTCCAGAGGGGG
ENST00000528981.5:c.491_492insGGCCTTATTCCAGAGGGGG
ENST00000529364.1:c.750_751insGGCCTTATTCCAGAGGGGG
ENST00000532635.5:c.691_692insGGCCTTATTCCAGAGGGGG	ENSP00000434407.1:p.Leu231ArgfsTer?
ENST00000533005.5:n.375_376insGGCCTTATTCCAGAGGGGG
NM_006019.3:c.1339_1340insGGCCTTATTCCAGAGGGGG	NP_006010.2:p.Leu447ArgfsTer?
NM_006053.3:c.691_692insGGCCTTATTCCAGAGGGGG	NP_006044.1:p.Leu231ArgfsTer?
XM_005273709.2:c.1339_1340insGGCCTTATTCCAGAGGGGG	XP_005273766.1:p.Leu447ArgfsTer?
XM_011544726.1:c.1339_1340insGGCCTTATTCCAGAGGGGG	XP_011543028.1:p.Leu447ArgfsTer?
XM_011544727.1:c.1339_1340insGGCCTTATTCCAGAGGGGG	XP_011543029.1:p.Leu447ArgfsTer?
XM_011544728.1:c.1339_1340insGGCCTTATTCCAGAGGGGG	XP_011543030.1:p.Leu447ArgfsTer?
XM_011544729.1:c.1355_1356insGGCCTTATTCCAGAGGGGG	XP_011543031.1:p.Pro453AlafsTer?
XR_949754.1:n.1343_1344insGGCCTTATTCCAGAGGGGG
NM_001351059.1:c.445_446insGGCCTTATTCCAGAGGGGG	NP_001337988.1:p.Leu149ArgfsTer?
XM_024448320.1:c.1355_1356insGGCCTTATTCCAGAGGGGG	XP_024304088.1:p.Pro453AlafsTer?
XM_024448321.1:c.1355_1356insGGCCTTATTCCAGAGGGGG	XP_024304089.1:p.Pro453AlafsTer?
XM_024448322.1:c.1355_1356insGGCCTTATTCCAGAGGGGG	XP_024304090.1:p.Pro453AlafsTer?
XM_024448323.1:c.1355_1356insGGCCTTATTCCAGAGGGGG	XP_024304091.1:p.Pro453AlafsTer?
XM_024448324.1:c.1355_1356insGGCCTTATTCCAGAGGGGG	XP_024304092.1:p.Pro453AlafsTer?
XR_001747721.2:n.1463_1464insGGCCTTATTCCAGAGGGGG
XR_001747722.1:n.1476_1477insGGCCTTATTCCAGAGGGGG
XR_001747723.2:n.1476_1477insGGCCTTATTCCAGAGGGGG
XR_002957115.1:n.1477_1478insGGCCTTATTCCAGAGGGGG
NM_006019.4:c.1339_1340insGGCCTTATTCCAGAGGGGG MANE Select	NP_006010.2:p.Leu447ArgfsTer?
NM_001351059.2:c.445_446insGGCCTTATTCCAGAGGGGG	NP_001337988.1:p.Leu149ArgfsTer?
NM_006053.4:c.691_692insGGCCTTATTCCAGAGGGGG	NP_006044.1:p.Leu231ArgfsTer?