Canonical Allele Identifier: CA1980430016

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047908T= , CM000673.2:g.68047908T=	GRCh38
NC_000011.9:g.67815375T= , CM000673.1:g.67815375T=	GRCh37
NC_000011.8:g.67571951T=	NCBI36
NG_007878.1:g.13893T= , LRG_115:g.13893T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.115T=
ENST00000698254.1:c.1019T=	ENSP00000513629.1:p.Met340=
ENST00000698255.1:c.1439T=	ENSP00000513630.1:p.Met480=
ENST00000698256.1:c.956T=
ENST00000698257.1:n.908T=
ENST00000698258.1:n.625T=
ENST00000698259.1:n.391T=
ENST00000265686.8:c.1490T= MANE Select	ENSP00000265686.3:p.Met497=
ENST00000265686.7:c.1490T=	ENSP00000265686.3:p.Met497=
ENST00000525516.1:n.284T=
ENST00000525724.5:n.802T=
ENST00000528981.5:c.642T=
ENST00000532635.5:c.842T=	ENSP00000434407.1:p.Met281=
ENST00000533005.5:n.603T=
NM_006019.3:c.1490T=	NP_006010.2:p.Met497=
NM_006053.3:c.842T=	NP_006044.1:p.Met281=
XM_005273709.2:c.1490T=	XP_005273766.1:p.Met497=
XM_011544726.1:c.1490T=	XP_011543028.1:p.Met497=
XM_011544727.1:c.1490T=	XP_011543029.1:p.Met497=
XM_011544728.1:c.1490T=	XP_011543030.1:p.Met497=
XR_949754.1:n.1494T=
NM_001351059.1:c.596T=	NP_001337988.1:p.Met199=
XM_024448320.1:c.1583T=	XP_024304088.1:p.Met528=
XM_024448321.1:c.1583T=	XP_024304089.1:p.Met528=
XM_024448322.1:c.1583T=	XP_024304090.1:p.Met528=
XM_024448323.1:c.1583T=	XP_024304091.1:p.Met528=
XM_024448324.1:c.1583T=	XP_024304092.1:p.Met528=
XR_001747721.2:n.1614T=
XR_001747722.1:n.1627T=
XR_001747723.2:n.1627T=
XR_002957115.1:n.1705T=
NM_006019.4:c.1490T= MANE Select	NP_006010.2:p.Met497=
NM_001351059.2:c.596T=	NP_001337988.1:p.Met199=
NM_006053.4:c.842T=	NP_006044.1:p.Met281=