Canonical Allele Identifier: CA2614700468

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047928-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047929dup , CM000673.2:g.68047929dup	GRCh38
NC_000011.9:g.67815396dup , CM000673.1:g.67815396dup	GRCh37
NC_000011.8:g.67571972dup	NCBI36
NG_007878.1:g.13914dup , LRG_115:g.13914dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.136dup
ENST00000698254.1:c.1040dup	ENSP00000513629.1:p.Thr348HisfsTer?
ENST00000698255.1:c.1460dup	ENSP00000513630.1:p.Thr488HisfsTer?
ENST00000698256.1:c.977dup
ENST00000698257.1:n.929dup
ENST00000698258.1:n.646dup
ENST00000698259.1:n.412dup
ENST00000265686.8:c.1511dup MANE Select	ENSP00000265686.3:p.Thr505HisfsTer?
ENST00000265686.7:c.1511dup	ENSP00000265686.3:p.Thr505HisfsTer?
ENST00000525516.1:n.305dup
ENST00000525724.5:n.823dup
ENST00000528981.5:c.663dup
ENST00000532635.5:c.863dup	ENSP00000434407.1:p.Thr289HisfsTer?
ENST00000533005.5:n.624dup
NM_006019.3:c.1511dup	NP_006010.2:p.Thr505HisfsTer?
NM_006053.3:c.863dup	NP_006044.1:p.Thr289HisfsTer?
XM_005273709.2:c.1511dup	XP_005273766.1:p.Thr505HisfsTer?
XM_011544726.1:c.1511dup	XP_011543028.1:p.Thr505HisfsTer?
XM_011544727.1:c.1511dup	XP_011543029.1:p.Thr505HisfsTer?
XM_011544728.1:c.1511dup	XP_011543030.1:p.Thr505HisfsTer?
XR_949754.1:n.1515dup
NM_001351059.1:c.617dup	NP_001337988.1:p.Thr207HisfsTer?
XM_024448320.1:c.1604dup	XP_024304088.1:p.Thr536HisfsTer?
XM_024448321.1:c.1604dup	XP_024304089.1:p.Thr536HisfsTer?
XM_024448322.1:c.1604dup	XP_024304090.1:p.Thr536HisfsTer?
XM_024448323.1:c.1604dup	XP_024304091.1:p.Thr536HisfsTer?
XM_024448324.1:c.1604dup	XP_024304092.1:p.Thr536HisfsTer?
XR_001747721.2:n.1635dup
XR_001747722.1:n.1648dup
XR_001747723.2:n.1648dup
XR_002957115.1:n.1726dup
NM_006019.4:c.1511dup MANE Select	NP_006010.2:p.Thr505HisfsTer?
NM_001351059.2:c.617dup	NP_001337988.1:p.Thr207HisfsTer?
NM_006053.4:c.863dup	NP_006044.1:p.Thr289HisfsTer?