Canonical Allele Identifier: CA1980432064

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048887C= , CM000673.2:g.68048887C=	GRCh38
NC_000011.9:g.67816354C= , CM000673.1:g.67816354C=	GRCh37
NC_000011.8:g.67572930C=	NCBI36
NG_007878.1:g.14872C= , LRG_115:g.14872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.188C=
ENST00000698254.1:c.1092C=	ENSP00000513629.1:p.Ser364=
ENST00000698255.1:c.1512C=	ENSP00000513630.1:p.Ser504=
ENST00000698256.1:c.1029C=
ENST00000698257.1:n.981C=
ENST00000698258.1:n.698C=
ENST00000698259.1:n.464C=
ENST00000265686.8:c.1563C= MANE Select	ENSP00000265686.3:p.Ser521=
ENST00000265686.7:c.1563C=	ENSP00000265686.3:p.Ser521=
ENST00000525724.5:n.875C=
ENST00000528981.5:c.715C=
ENST00000532635.5:c.915C=	ENSP00000434407.1:p.Ser305=
ENST00000533005.5:n.676C=
NM_006019.3:c.1563C=	NP_006010.2:p.Ser521=
NM_006053.3:c.915C=	NP_006044.1:p.Ser305=
XM_005273709.2:c.1563C=	XP_005273766.1:p.Ser521=
XM_011544726.1:c.1563C=	XP_011543028.1:p.Ser521=
XM_011544727.1:c.1563C=	XP_011543029.1:p.Ser521=
XM_011544728.1:c.1563C=	XP_011543030.1:p.Ser521=
XR_949754.1:n.1567C=
NM_001351059.1:c.669C=	NP_001337988.1:p.Ser223=
XM_024448320.1:c.1656C=	XP_024304088.1:p.Ser552=
XM_024448321.1:c.1656C=	XP_024304089.1:p.Ser552=
XM_024448322.1:c.1656C=	XP_024304090.1:p.Ser552=
XM_024448323.1:c.1656C=	XP_024304091.1:p.Ser552=
XM_024448324.1:c.1656C=	XP_024304092.1:p.Ser552=
XR_001747721.2:n.1687C=
XR_001747722.1:n.1700C=
XR_001747723.2:n.1700C=
XR_002957115.1:n.1778C=
NM_006019.4:c.1563C= MANE Select	NP_006010.2:p.Ser521=
NM_001351059.2:c.669C=	NP_001337988.1:p.Ser223=
NM_006053.4:c.915C=	NP_006044.1:p.Ser305=