Canonical Allele Identifier: CA1980429456

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047689A= , CM000673.2:g.68047689A=	GRCh38
NC_000011.9:g.67815156A= , CM000673.1:g.67815156A=	GRCh37
NC_000011.8:g.67571732A=	NCBI36
NG_007878.1:g.13674A= , LRG_115:g.13674A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.877A=	ENSP00000513629.1:p.Met293=
ENST00000698255.1:c.1297A=	ENSP00000513630.1:p.Met433=
ENST00000698256.1:c.814A=
ENST00000698257.1:n.766A=
ENST00000698258.1:n.406A=
ENST00000698259.1:n.172A=
ENST00000265686.8:c.1348A= MANE Select	ENSP00000265686.3:p.Met450=
ENST00000265686.7:c.1348A=	ENSP00000265686.3:p.Met450=
ENST00000525516.1:n.142A=
ENST00000525724.5:n.660A=
ENST00000528981.5:c.500A=
ENST00000529364.1:c.759A=
ENST00000532635.5:c.700A=	ENSP00000434407.1:p.Met234=
ENST00000533005.5:n.384A=
NM_006019.3:c.1348A=	NP_006010.2:p.Met450=
NM_006053.3:c.700A=	NP_006044.1:p.Met234=
XM_005273709.2:c.1348A=	XP_005273766.1:p.Met450=
XM_011544726.1:c.1348A=	XP_011543028.1:p.Met450=
XM_011544727.1:c.1348A=	XP_011543029.1:p.Met450=
XM_011544728.1:c.1348A=	XP_011543030.1:p.Met450=
XM_011544729.1:c.1364A=	XP_011543031.1:p.Tyr455=
XR_949754.1:n.1352A=
NM_001351059.1:c.454A=	NP_001337988.1:p.Met152=
XM_024448320.1:c.1364A=	XP_024304088.1:p.Tyr455=
XM_024448321.1:c.1364A=	XP_024304089.1:p.Tyr455=
XM_024448322.1:c.1364A=	XP_024304090.1:p.Tyr455=
XM_024448323.1:c.1364A=	XP_024304091.1:p.Tyr455=
XM_024448324.1:c.1364A=	XP_024304092.1:p.Tyr455=
XR_001747721.2:n.1472A=
XR_001747722.1:n.1485A=
XR_001747723.2:n.1485A=
XR_002957115.1:n.1486A=
NM_006019.4:c.1348A= MANE Select	NP_006010.2:p.Met450=
NM_001351059.2:c.454A=	NP_001337988.1:p.Met152=
NM_006053.4:c.700A=	NP_006044.1:p.Met234=