Canonical Allele Identifier: CA1980430148

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047946G= , CM000673.2:g.68047946G=	GRCh38
NC_000011.9:g.67815413G= , CM000673.1:g.67815413G=	GRCh37
NC_000011.8:g.67571989G=	NCBI36
NG_007878.1:g.13931G= , LRG_115:g.13931G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.153G=
ENST00000698254.1:c.1057G=	ENSP00000513629.1:p.Gly353=
ENST00000698255.1:c.1477G=	ENSP00000513630.1:p.Gly493=
ENST00000698256.1:c.994G=
ENST00000698257.1:n.946G=
ENST00000698258.1:n.663G=
ENST00000698259.1:n.429G=
ENST00000265686.8:c.1528G= MANE Select	ENSP00000265686.3:p.Gly510=
ENST00000265686.7:c.1528G=	ENSP00000265686.3:p.Gly510=
ENST00000525516.1:n.322G=
ENST00000525724.5:n.840G=
ENST00000528981.5:c.680G=
ENST00000532635.5:c.880G=	ENSP00000434407.1:p.Gly294=
ENST00000533005.5:n.641G=
NM_006019.3:c.1528G=	NP_006010.2:p.Gly510=
NM_006053.3:c.880G=	NP_006044.1:p.Gly294=
XM_005273709.2:c.1528G=	XP_005273766.1:p.Gly510=
XM_011544726.1:c.1528G=	XP_011543028.1:p.Gly510=
XM_011544727.1:c.1528G=	XP_011543029.1:p.Gly510=
XM_011544728.1:c.1528G=	XP_011543030.1:p.Gly510=
XR_949754.1:n.1532G=
NM_001351059.1:c.634G=	NP_001337988.1:p.Gly212=
XM_024448320.1:c.1621G=	XP_024304088.1:p.Gly541=
XM_024448321.1:c.1621G=	XP_024304089.1:p.Gly541=
XM_024448322.1:c.1621G=	XP_024304090.1:p.Gly541=
XM_024448323.1:c.1621G=	XP_024304091.1:p.Gly541=
XM_024448324.1:c.1621G=	XP_024304092.1:p.Gly541=
XR_001747721.2:n.1652G=
XR_001747722.1:n.1665G=
XR_001747723.2:n.1665G=
XR_002957115.1:n.1743G=
NM_006019.4:c.1528G= MANE Select	NP_006010.2:p.Gly510=
NM_001351059.2:c.634G=	NP_001337988.1:p.Gly212=
NM_006053.4:c.880G=	NP_006044.1:p.Gly294=