Canonical Allele Identifier: CA1980429488

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047700C= , CM000673.2:g.68047700C=	GRCh38
NC_000011.9:g.67815167C= , CM000673.1:g.67815167C=	GRCh37
NC_000011.8:g.67571743C=	NCBI36
NG_007878.1:g.13685C= , LRG_115:g.13685C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.888C=	ENSP00000513629.1:p.Phe296=
ENST00000698255.1:c.1308C=	ENSP00000513630.1:p.Phe436=
ENST00000698256.1:c.825C=
ENST00000698257.1:n.777C=
ENST00000698258.1:n.417C=
ENST00000698259.1:n.183C=
ENST00000265686.8:c.1359C= MANE Select	ENSP00000265686.3:p.Phe453=
ENST00000265686.7:c.1359C=	ENSP00000265686.3:p.Phe453=
ENST00000525516.1:n.153C=
ENST00000525724.5:n.671C=
ENST00000528981.5:c.511C=
ENST00000529364.1:c.770C=
ENST00000532635.5:c.711C=	ENSP00000434407.1:p.Phe237=
ENST00000533005.5:n.395C=
NM_006019.3:c.1359C=	NP_006010.2:p.Phe453=
NM_006053.3:c.711C=	NP_006044.1:p.Phe237=
XM_005273709.2:c.1359C=	XP_005273766.1:p.Phe453=
XM_011544726.1:c.1359C=	XP_011543028.1:p.Phe453=
XM_011544727.1:c.1359C=	XP_011543029.1:p.Phe453=
XM_011544728.1:c.1359C=	XP_011543030.1:p.Phe453=
XM_011544729.1:c.1375C=	XP_011543031.1:p.Leu459=
XR_949754.1:n.1363C=
NM_001351059.1:c.465C=	NP_001337988.1:p.Phe155=
XM_024448320.1:c.1375C=	XP_024304088.1:p.Leu459=
XM_024448321.1:c.1375C=	XP_024304089.1:p.Leu459=
XM_024448322.1:c.1375C=	XP_024304090.1:p.Leu459=
XM_024448323.1:c.1375C=	XP_024304091.1:p.Leu459=
XM_024448324.1:c.1375C=	XP_024304092.1:p.Leu459=
XR_001747721.2:n.1483C=
XR_001747722.1:n.1496C=
XR_001747723.2:n.1496C=
XR_002957115.1:n.1497C=
NM_006019.4:c.1359C= MANE Select	NP_006010.2:p.Phe453=
NM_001351059.2:c.465C=	NP_001337988.1:p.Phe155=
NM_006053.4:c.711C=	NP_006044.1:p.Phe237=