Canonical Allele Identifier: CA1980428801

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047481G= , CM000673.2:g.68047481G=	GRCh38
NC_000011.9:g.67814948G= , CM000673.1:g.67814948G=	GRCh37
NC_000011.8:g.67571524G=	NCBI36
NG_007878.1:g.13466G= , LRG_115:g.13466G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698254.1:c.743G=	ENSP00000513629.1:p.Gly248=
ENST00000698255.1:c.1163G=	ENSP00000513630.1:p.Gly388=
ENST00000698256.1:c.680G=
ENST00000698257.1:n.632G=
ENST00000698258.1:n.198G=
ENST00000698259.1:n.38G=
ENST00000265686.8:c.1214G= MANE Select	ENSP00000265686.3:p.Gly405=
ENST00000265686.7:c.1214G=	ENSP00000265686.3:p.Gly405=
ENST00000525516.1:n.8G=
ENST00000525724.5:n.526G=
ENST00000528981.5:c.366G=
ENST00000529364.1:c.625G=
ENST00000532635.5:c.566G=	ENSP00000434407.1:p.Gly189=
ENST00000533005.5:n.250G=
NM_006019.3:c.1214G=	NP_006010.2:p.Gly405=
NM_006053.3:c.566G=	NP_006044.1:p.Gly189=
XM_005273709.2:c.1214G=	XP_005273766.1:p.Gly405=
XM_011544726.1:c.1214G=	XP_011543028.1:p.Gly405=
XM_011544727.1:c.1214G=	XP_011543029.1:p.Gly405=
XM_011544728.1:c.1214G=	XP_011543030.1:p.Gly405=
XM_011544729.1:c.1230G=	XP_011543031.1:p.Arg410=
XR_949754.1:n.1218G=
NM_001351059.1:c.320G=	NP_001337988.1:p.Gly107=
XM_024448320.1:c.1230G=	XP_024304088.1:p.Arg410=
XM_024448321.1:c.1230G=	XP_024304089.1:p.Arg410=
XM_024448322.1:c.1230G=	XP_024304090.1:p.Arg410=
XM_024448323.1:c.1230G=	XP_024304091.1:p.Arg410=
XM_024448324.1:c.1230G=	XP_024304092.1:p.Arg410=
XR_001747721.2:n.1338G=
XR_001747722.1:n.1351G=
XR_001747723.2:n.1351G=
XR_002957115.1:n.1352G=
NM_006019.4:c.1214G= MANE Select	NP_006010.2:p.Gly405=
NM_001351059.2:c.320G=	NP_001337988.1:p.Gly107=
NM_006053.4:c.566G=	NP_006044.1:p.Gly189=