Canonical Allele Identifier: CA1980428794

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047480G= , CM000673.2:g.68047480G=	GRCh38
NC_000011.9:g.67814947G= , CM000673.1:g.67814947G=	GRCh37
NC_000011.8:g.67571523G=	NCBI36
NG_007878.1:g.13465G= , LRG_115:g.13465G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.742G=	ENSP00000513629.1:p.Gly248=
ENST00000698255.1:c.1162G=	ENSP00000513630.1:p.Gly388=
ENST00000698256.1:c.679G=
ENST00000698257.1:n.631G=
ENST00000698258.1:n.197G=
ENST00000698259.1:n.37G=
ENST00000265686.8:c.1213G= MANE Select	ENSP00000265686.3:p.Gly405=
ENST00000265686.7:c.1213G=	ENSP00000265686.3:p.Gly405=
ENST00000525516.1:n.7G=
ENST00000525724.5:n.525G=
ENST00000528981.5:c.365G=
ENST00000529364.1:c.624G=
ENST00000532635.5:c.565G=	ENSP00000434407.1:p.Gly189=
ENST00000533005.5:n.249G=
NM_006019.3:c.1213G=	NP_006010.2:p.Gly405=
NM_006053.3:c.565G=	NP_006044.1:p.Gly189=
XM_005273709.2:c.1213G=	XP_005273766.1:p.Gly405=
XM_011544726.1:c.1213G=	XP_011543028.1:p.Gly405=
XM_011544727.1:c.1213G=	XP_011543029.1:p.Gly405=
XM_011544728.1:c.1213G=	XP_011543030.1:p.Gly405=
XM_011544729.1:c.1229G=	XP_011543031.1:p.Arg410=
XR_949754.1:n.1217G=
NM_001351059.1:c.319G=	NP_001337988.1:p.Gly107=
XM_024448320.1:c.1229G=	XP_024304088.1:p.Arg410=
XM_024448321.1:c.1229G=	XP_024304089.1:p.Arg410=
XM_024448322.1:c.1229G=	XP_024304090.1:p.Arg410=
XM_024448323.1:c.1229G=	XP_024304091.1:p.Arg410=
XM_024448324.1:c.1229G=	XP_024304092.1:p.Arg410=
XR_001747721.2:n.1337G=
XR_001747722.1:n.1350G=
XR_001747723.2:n.1350G=
XR_002957115.1:n.1351G=
NM_006019.4:c.1213G= MANE Select	NP_006010.2:p.Gly405=
NM_001351059.2:c.319G=	NP_001337988.1:p.Gly107=
NM_006053.4:c.565G=	NP_006044.1:p.Gly189=