Canonical Allele Identifier: CA1980429971

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047898C= , CM000673.2:g.68047898C=	GRCh38
NC_000011.9:g.67815365C= , CM000673.1:g.67815365C=	GRCh37
NC_000011.8:g.67571941C=	NCBI36
NG_007878.1:g.13883C= , LRG_115:g.13883C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.105C=
ENST00000698254.1:c.1009C=	ENSP00000513629.1:p.Gln337=
ENST00000698255.1:c.1429C=	ENSP00000513630.1:p.Gln477=
ENST00000698256.1:c.946C=
ENST00000698257.1:n.898C=
ENST00000698258.1:n.615C=
ENST00000698259.1:n.381C=
ENST00000265686.8:c.1480C= MANE Select	ENSP00000265686.3:p.Gln494=
ENST00000265686.7:c.1480C=	ENSP00000265686.3:p.Gln494=
ENST00000525516.1:n.274C=
ENST00000525724.5:n.792C=
ENST00000528981.5:c.632C=
ENST00000532635.5:c.832C=	ENSP00000434407.1:p.Gln278=
ENST00000533005.5:n.593C=
NM_006019.3:c.1480C=	NP_006010.2:p.Gln494=
NM_006053.3:c.832C=	NP_006044.1:p.Gln278=
XM_005273709.2:c.1480C=	XP_005273766.1:p.Gln494=
XM_011544726.1:c.1480C=	XP_011543028.1:p.Gln494=
XM_011544727.1:c.1480C=	XP_011543029.1:p.Gln494=
XM_011544728.1:c.1480C=	XP_011543030.1:p.Gln494=
XR_949754.1:n.1484C=
NM_001351059.1:c.586C=	NP_001337988.1:p.Gln196=
XM_024448320.1:c.1573C=	XP_024304088.1:p.Gln525=
XM_024448321.1:c.1573C=	XP_024304089.1:p.Gln525=
XM_024448322.1:c.1573C=	XP_024304090.1:p.Gln525=
XM_024448323.1:c.1573C=	XP_024304091.1:p.Gln525=
XM_024448324.1:c.1573C=	XP_024304092.1:p.Gln525=
XR_001747721.2:n.1604C=
XR_001747722.1:n.1617C=
XR_001747723.2:n.1617C=
XR_002957115.1:n.1695C=
NM_006019.4:c.1480C= MANE Select	NP_006010.2:p.Gln494=
NM_001351059.2:c.586C=	NP_001337988.1:p.Gln196=
NM_006053.4:c.832C=	NP_006044.1:p.Gln278=