Canonical Allele Identifier: CA1980430131

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047939C= , CM000673.2:g.68047939C=	GRCh38
NC_000011.9:g.67815406C= , CM000673.1:g.67815406C=	GRCh37
NC_000011.8:g.67571982C=	NCBI36
NG_007878.1:g.13924C= , LRG_115:g.13924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.146C=
ENST00000698254.1:c.1050C=	ENSP00000513629.1:p.Val350=
ENST00000698255.1:c.1470C=	ENSP00000513630.1:p.Val490=
ENST00000698256.1:c.987C=
ENST00000698257.1:n.939C=
ENST00000698258.1:n.656C=
ENST00000698259.1:n.422C=
ENST00000265686.8:c.1521C= MANE Select	ENSP00000265686.3:p.Val507=
ENST00000265686.7:c.1521C=	ENSP00000265686.3:p.Val507=
ENST00000525516.1:n.315C=
ENST00000525724.5:n.833C=
ENST00000528981.5:c.673C=
ENST00000532635.5:c.873C=	ENSP00000434407.1:p.Val291=
ENST00000533005.5:n.634C=
NM_006019.3:c.1521C=	NP_006010.2:p.Val507=
NM_006053.3:c.873C=	NP_006044.1:p.Val291=
XM_005273709.2:c.1521C=	XP_005273766.1:p.Val507=
XM_011544726.1:c.1521C=	XP_011543028.1:p.Val507=
XM_011544727.1:c.1521C=	XP_011543029.1:p.Val507=
XM_011544728.1:c.1521C=	XP_011543030.1:p.Val507=
XR_949754.1:n.1525C=
NM_001351059.1:c.627C=	NP_001337988.1:p.Val209=
XM_024448320.1:c.1614C=	XP_024304088.1:p.Val538=
XM_024448321.1:c.1614C=	XP_024304089.1:p.Val538=
XM_024448322.1:c.1614C=	XP_024304090.1:p.Val538=
XM_024448323.1:c.1614C=	XP_024304091.1:p.Val538=
XM_024448324.1:c.1614C=	XP_024304092.1:p.Val538=
XR_001747721.2:n.1645C=
XR_001747722.1:n.1658C=
XR_001747723.2:n.1658C=
XR_002957115.1:n.1736C=
NM_006019.4:c.1521C= MANE Select	NP_006010.2:p.Val507=
NM_001351059.2:c.627C=	NP_001337988.1:p.Val209=
NM_006053.4:c.873C=	NP_006044.1:p.Val291=