Canonical Allele Identifier: CA1980429554

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047719A= , CM000673.2:g.68047719A=	GRCh38
NC_000011.9:g.67815186A= , CM000673.1:g.67815186A=	GRCh37
NC_000011.8:g.67571762A=	NCBI36
NG_007878.1:g.13704A= , LRG_115:g.13704A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.3A=
ENST00000698254.1:c.907A=	ENSP00000513629.1:p.Ile303=
ENST00000698255.1:c.1327A=	ENSP00000513630.1:p.Ile443=
ENST00000698256.1:c.844A=
ENST00000698257.1:n.796A=
ENST00000698258.1:n.436A=
ENST00000698259.1:n.202A=
ENST00000265686.8:c.1378A= MANE Select	ENSP00000265686.3:p.Ile460=
ENST00000265686.7:c.1378A=	ENSP00000265686.3:p.Ile460=
ENST00000525516.1:n.172A=
ENST00000525724.5:n.690A=
ENST00000528981.5:c.530A=
ENST00000529364.1:c.789A=
ENST00000532635.5:c.730A=	ENSP00000434407.1:p.Ile244=
ENST00000533005.5:n.414A=
NM_006019.3:c.1378A=	NP_006010.2:p.Ile460=
NM_006053.3:c.730A=	NP_006044.1:p.Ile244=
XM_005273709.2:c.1378A=	XP_005273766.1:p.Ile460=
XM_011544726.1:c.1378A=	XP_011543028.1:p.Ile460=
XM_011544727.1:c.1378A=	XP_011543029.1:p.Ile460=
XM_011544728.1:c.1378A=	XP_011543030.1:p.Ile460=
XM_011544729.1:c.1394A=	XP_011543031.1:p.His465=
XR_949754.1:n.1382A=
NM_001351059.1:c.484A=	NP_001337988.1:p.Ile162=
XM_024448320.1:c.1394A=	XP_024304088.1:p.His465=
XM_024448321.1:c.1394A=	XP_024304089.1:p.His465=
XM_024448322.1:c.1394A=	XP_024304090.1:p.His465=
XM_024448323.1:c.1394A=	XP_024304091.1:p.His465=
XM_024448324.1:c.1394A=	XP_024304092.1:p.His465=
XR_001747721.2:n.1502A=
XR_001747722.1:n.1515A=
XR_001747723.2:n.1515A=
XR_002957115.1:n.1516A=
NM_006019.4:c.1378A= MANE Select	NP_006010.2:p.Ile460=
NM_001351059.2:c.484A=	NP_001337988.1:p.Ile162=
NM_006053.4:c.730A=	NP_006044.1:p.Ile244=