Canonical Allele Identifier: CA1980429394

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047671C= , CM000673.2:g.68047671C=	GRCh38
NC_000011.9:g.67815138C= , CM000673.1:g.67815138C=	GRCh37
NC_000011.8:g.67571714C=	NCBI36
NG_007878.1:g.13656C= , LRG_115:g.13656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.859C=	ENSP00000513629.1:p.Arg287=
ENST00000698255.1:c.1279C=	ENSP00000513630.1:p.Arg427=
ENST00000698256.1:c.796C=
ENST00000698257.1:n.748C=
ENST00000698258.1:n.388C=
ENST00000698259.1:n.154C=
ENST00000265686.8:c.1330C= MANE Select	ENSP00000265686.3:p.Arg444=
ENST00000265686.7:c.1330C=	ENSP00000265686.3:p.Arg444=
ENST00000525516.1:n.124C=
ENST00000525724.5:n.642C=
ENST00000528981.5:c.482C=
ENST00000529364.1:c.741C=
ENST00000532635.5:c.682C=	ENSP00000434407.1:p.Arg228=
ENST00000533005.5:n.366C=
NM_006019.3:c.1330C=	NP_006010.2:p.Arg444=
NM_006053.3:c.682C=	NP_006044.1:p.Arg228=
XM_005273709.2:c.1330C=	XP_005273766.1:p.Arg444=
XM_011544726.1:c.1330C=	XP_011543028.1:p.Arg444=
XM_011544727.1:c.1330C=	XP_011543029.1:p.Arg444=
XM_011544728.1:c.1330C=	XP_011543030.1:p.Arg444=
XM_011544729.1:c.1346C=	XP_011543031.1:p.Pro449=
XR_949754.1:n.1334C=
NM_001351059.1:c.436C=	NP_001337988.1:p.Arg146=
XM_024448320.1:c.1346C=	XP_024304088.1:p.Pro449=
XM_024448321.1:c.1346C=	XP_024304089.1:p.Pro449=
XM_024448322.1:c.1346C=	XP_024304090.1:p.Pro449=
XM_024448323.1:c.1346C=	XP_024304091.1:p.Pro449=
XM_024448324.1:c.1346C=	XP_024304092.1:p.Pro449=
XR_001747721.2:n.1454C=
XR_001747722.1:n.1467C=
XR_001747723.2:n.1467C=
XR_002957115.1:n.1468C=
NM_006019.4:c.1330C= MANE Select	NP_006010.2:p.Arg444=
NM_001351059.2:c.436C=	NP_001337988.1:p.Arg146=
NM_006053.4:c.682C=	NP_006044.1:p.Arg228=