Canonical Allele Identifier: CA1980430091

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047929T= , CM000673.2:g.68047929T=	GRCh38
NC_000011.9:g.67815396T= , CM000673.1:g.67815396T=	GRCh37
NC_000011.8:g.67571972T=	NCBI36
NG_007878.1:g.13914T= , LRG_115:g.13914T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.136T=
ENST00000698254.1:c.1040T=	ENSP00000513629.1:p.Val347=
ENST00000698255.1:c.1460T=	ENSP00000513630.1:p.Val487=
ENST00000698256.1:c.977T=
ENST00000698257.1:n.929T=
ENST00000698258.1:n.646T=
ENST00000698259.1:n.412T=
ENST00000265686.8:c.1511T= MANE Select	ENSP00000265686.3:p.Val504=
ENST00000265686.7:c.1511T=	ENSP00000265686.3:p.Val504=
ENST00000525516.1:n.305T=
ENST00000525724.5:n.823T=
ENST00000528981.5:c.663T=
ENST00000532635.5:c.863T=	ENSP00000434407.1:p.Val288=
ENST00000533005.5:n.624T=
NM_006019.3:c.1511T=	NP_006010.2:p.Val504=
NM_006053.3:c.863T=	NP_006044.1:p.Val288=
XM_005273709.2:c.1511T=	XP_005273766.1:p.Val504=
XM_011544726.1:c.1511T=	XP_011543028.1:p.Val504=
XM_011544727.1:c.1511T=	XP_011543029.1:p.Val504=
XM_011544728.1:c.1511T=	XP_011543030.1:p.Val504=
XR_949754.1:n.1515T=
NM_001351059.1:c.617T=	NP_001337988.1:p.Val206=
XM_024448320.1:c.1604T=	XP_024304088.1:p.Val535=
XM_024448321.1:c.1604T=	XP_024304089.1:p.Val535=
XM_024448322.1:c.1604T=	XP_024304090.1:p.Val535=
XM_024448323.1:c.1604T=	XP_024304091.1:p.Val535=
XM_024448324.1:c.1604T=	XP_024304092.1:p.Val535=
XR_001747721.2:n.1635T=
XR_001747722.1:n.1648T=
XR_001747723.2:n.1648T=
XR_002957115.1:n.1726T=
NM_006019.4:c.1511T= MANE Select	NP_006010.2:p.Val504=
NM_001351059.2:c.617T=	NP_001337988.1:p.Val206=
NM_006053.4:c.863T=	NP_006044.1:p.Val288=