Canonical Allele Identifier: CA1980429670

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047768G= , CM000673.2:g.68047768G=	GRCh38
NC_000011.9:g.67815235G= , CM000673.1:g.67815235G=	GRCh37
NC_000011.8:g.67571811G=	NCBI36
NG_007878.1:g.13753G= , LRG_115:g.13753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.52G=
ENST00000698254.1:c.956G=	ENSP00000513629.1:p.Trp319=
ENST00000698255.1:c.1376G=	ENSP00000513630.1:p.Trp459=
ENST00000698256.1:c.893G=
ENST00000698257.1:n.845G=
ENST00000698258.1:n.485G=
ENST00000698259.1:n.251G=
ENST00000265686.8:c.1427G= MANE Select	ENSP00000265686.3:p.Trp476=
ENST00000265686.7:c.1427G=	ENSP00000265686.3:p.Trp476=
ENST00000525516.1:n.221G=
ENST00000525724.5:n.739G=
ENST00000528981.5:c.579G=
ENST00000529364.1:c.838G=
ENST00000532635.5:c.779G=	ENSP00000434407.1:p.Trp260=
ENST00000533005.5:n.463G=
NM_006019.3:c.1427G=	NP_006010.2:p.Trp476=
NM_006053.3:c.779G=	NP_006044.1:p.Trp260=
XM_005273709.2:c.1427G=	XP_005273766.1:p.Trp476=
XM_011544726.1:c.1427G=	XP_011543028.1:p.Trp476=
XM_011544727.1:c.1427G=	XP_011543029.1:p.Trp476=
XM_011544728.1:c.1427G=	XP_011543030.1:p.Trp476=
XM_011544729.1:c.1443G=	XP_011543031.1:p.Leu481=
XR_949754.1:n.1431G=
NM_001351059.1:c.533G=	NP_001337988.1:p.Trp178=
XM_024448320.1:c.1443G=	XP_024304088.1:p.Leu481=
XM_024448321.1:c.1443G=	XP_024304089.1:p.Leu481=
XM_024448322.1:c.1443G=	XP_024304090.1:p.Leu481=
XM_024448323.1:c.1443G=	XP_024304091.1:p.Leu481=
XM_024448324.1:c.1443G=	XP_024304092.1:p.Leu481=
XR_001747721.2:n.1551G=
XR_001747722.1:n.1564G=
XR_001747723.2:n.1564G=
XR_002957115.1:n.1565G=
NM_006019.4:c.1427G= MANE Select	NP_006010.2:p.Trp476=
NM_001351059.2:c.533G=	NP_001337988.1:p.Trp178=
NM_006053.4:c.779G=	NP_006044.1:p.Trp260=