Canonical Allele Identifier: CA2614698837

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047479-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047483del , CM000673.2:g.68047483del	GRCh38
NC_000011.9:g.67814950del , CM000673.1:g.67814950del	GRCh37
NC_000011.8:g.67571526del	NCBI36
NG_007878.1:g.13468del , LRG_115:g.13468del

Transcript Alleles

HGVS	Amino-acid change
ENST00000698254.1:c.745del	ENSP00000513629.1:p.Asp249MetfsTer24
ENST00000698255.1:c.1165del	ENSP00000513630.1:p.Asp389MetfsTer24
ENST00000698256.1:c.682del
ENST00000698257.1:n.634del
ENST00000698258.1:n.200del
ENST00000698259.1:n.40del
ENST00000265686.8:c.1216del MANE Select	ENSP00000265686.3:p.Asp406MetfsTer24
ENST00000265686.7:c.1216del	ENSP00000265686.3:p.Asp406MetfsTer24
ENST00000525516.1:n.10del
ENST00000525724.5:n.528del
ENST00000528981.5:c.368del
ENST00000529364.1:c.627del
ENST00000532635.5:c.568del	ENSP00000434407.1:p.Asp190MetfsTer24
ENST00000533005.5:n.252del
NM_006019.3:c.1216del	NP_006010.2:p.Asp406MetfsTer24
NM_006053.3:c.568del	NP_006044.1:p.Asp190MetfsTer24
XM_005273709.2:c.1216del	XP_005273766.1:p.Asp406MetfsTer24
XM_011544726.1:c.1216del	XP_011543028.1:p.Asp406MetfsTer24
XM_011544727.1:c.1216del	XP_011543029.1:p.Asp406MetfsTer24
XM_011544728.1:c.1216del	XP_011543030.1:p.Asp406MetfsTer24
XM_011544729.1:c.1232del	XP_011543031.1:p.Gly411AspfsTer?
XR_949754.1:n.1220del
NM_001351059.1:c.322del	NP_001337988.1:p.Asp108MetfsTer24
XM_024448320.1:c.1232del	XP_024304088.1:p.Gly411AspfsTer?
XM_024448321.1:c.1232del	XP_024304089.1:p.Gly411AspfsTer?
XM_024448322.1:c.1232del	XP_024304090.1:p.Gly411AspfsTer?
XM_024448323.1:c.1232del	XP_024304091.1:p.Gly411AspfsTer?
XM_024448324.1:c.1232del	XP_024304092.1:p.Gly411AspfsTer?
XR_001747721.2:n.1340del
XR_001747722.1:n.1353del
XR_001747723.2:n.1353del
XR_002957115.1:n.1354del
NM_006019.4:c.1216del MANE Select	NP_006010.2:p.Asp406MetfsTer24
NM_001351059.2:c.322del	NP_001337988.1:p.Asp108MetfsTer24
NM_006053.4:c.568del	NP_006044.1:p.Asp190MetfsTer24