Canonical Allele Identifier: CA1980436297

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050224C= , CM000673.2:g.68050224C=	GRCh38
NC_000011.9:g.67817691C= , CM000673.1:g.67817691C=	GRCh37
NC_000011.8:g.67574267C=	NCBI36
NG_007878.1:g.16209C= , LRG_115:g.16209C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2206C= MANE Select	NP_006010.2:p.Arg736=
ENST00000265686.8:c.2206C= MANE Select	ENSP00000265686.3:p.Arg736=
NM_001351059.1:c.1312C=	NP_001337988.1:p.Arg438=
NM_001351059.2:c.1312C=	NP_001337988.1:p.Arg438=
NM_006019.3:c.2206C=	NP_006010.2:p.Arg736=
NM_006053.3:c.1558C=	NP_006044.1:p.Arg520=
NM_006053.4:c.1558C=	NP_006044.1:p.Arg520=
ENST00000265686.7:c.2206C=	ENSP00000265686.3:p.Arg736=
ENST00000525724.5:n.1518C=
ENST00000530063.1:c.109C=	ENSP00000432957.1:p.Arg37=
ENST00000530449.1:n.102C=
ENST00000530449.2:n.1199C=
ENST00000532635.5:c.1558C=	ENSP00000434407.1:p.Arg520=
ENST00000533005.5:n.1319C=
ENST00000698254.1:c.1735C=	ENSP00000513629.1:p.Arg579=
ENST00000698255.1:c.2155C=	ENSP00000513630.1:p.Arg719=
ENST00000698256.1:c.1672C=
ENST00000698257.1:n.1624C=
ENST00000698258.1:n.1341C=
ENST00000698259.1:n.1475C=
XM_005273709.2:c.2206C=	XP_005273766.1:p.Arg736=
XM_011544726.1:c.2206C=	XP_011543028.1:p.Arg736=
XM_011544727.1:c.2206C=	XP_011543029.1:p.Arg736=
XM_024448320.1:c.2299C=	XP_024304088.1:p.Arg767=
XM_024448321.1:c.2299C=	XP_024304089.1:p.Arg767=
XM_024448322.1:c.2299C=	XP_024304090.1:p.Arg767=
XM_024448323.1:c.2299C=	XP_024304091.1:p.Arg767=
XR_001747721.2:n.2375C=
XR_001747722.1:n.2343C=
XR_001747723.2:n.2388C=
XR_002957115.1:n.2564C=
XR_949754.1:n.2353C=