Canonical Allele Identifier: CA1980430085

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047928G= , CM000673.2:g.68047928G=	GRCh38
NC_000011.9:g.67815395G= , CM000673.1:g.67815395G=	GRCh37
NC_000011.8:g.67571971G=	NCBI36
NG_007878.1:g.13913G= , LRG_115:g.13913G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.135G=
ENST00000698254.1:c.1039G=	ENSP00000513629.1:p.Val347=
ENST00000698255.1:c.1459G=	ENSP00000513630.1:p.Val487=
ENST00000698256.1:c.976G=
ENST00000698257.1:n.928G=
ENST00000698258.1:n.645G=
ENST00000698259.1:n.411G=
ENST00000265686.8:c.1510G= MANE Select	ENSP00000265686.3:p.Val504=
ENST00000265686.7:c.1510G=	ENSP00000265686.3:p.Val504=
ENST00000525516.1:n.304G=
ENST00000525724.5:n.822G=
ENST00000528981.5:c.662G=
ENST00000532635.5:c.862G=	ENSP00000434407.1:p.Val288=
ENST00000533005.5:n.623G=
NM_006019.3:c.1510G=	NP_006010.2:p.Val504=
NM_006053.3:c.862G=	NP_006044.1:p.Val288=
XM_005273709.2:c.1510G=	XP_005273766.1:p.Val504=
XM_011544726.1:c.1510G=	XP_011543028.1:p.Val504=
XM_011544727.1:c.1510G=	XP_011543029.1:p.Val504=
XM_011544728.1:c.1510G=	XP_011543030.1:p.Val504=
XR_949754.1:n.1514G=
NM_001351059.1:c.616G=	NP_001337988.1:p.Val206=
XM_024448320.1:c.1603G=	XP_024304088.1:p.Val535=
XM_024448321.1:c.1603G=	XP_024304089.1:p.Val535=
XM_024448322.1:c.1603G=	XP_024304090.1:p.Val535=
XM_024448323.1:c.1603G=	XP_024304091.1:p.Val535=
XM_024448324.1:c.1603G=	XP_024304092.1:p.Val535=
XR_001747721.2:n.1634G=
XR_001747722.1:n.1647G=
XR_001747723.2:n.1647G=
XR_002957115.1:n.1725G=
NM_006019.4:c.1510G= MANE Select	NP_006010.2:p.Val504=
NM_001351059.2:c.616G=	NP_001337988.1:p.Val206=
NM_006053.4:c.862G=	NP_006044.1:p.Val288=