Canonical Allele Identifier: CA1980430270

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047984G= , CM000673.2:g.68047984G=	GRCh38
NC_000011.9:g.67815451G= , CM000673.1:g.67815451G=	GRCh37
NC_000011.8:g.67572027G=	NCBI36
NG_007878.1:g.13969G= , LRG_115:g.13969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.179+12G=
ENST00000698254.1:c.1083+12G=	ENSP00000513629.1:n.1083+12G=
ENST00000698255.1:c.1503+12G=	ENSP00000513630.1:n.1503+12G=
ENST00000698256.1:c.1020+12G=
ENST00000698257.1:n.972+12G=
ENST00000698258.1:n.689+12G=
ENST00000698259.1:n.455+12G=
ENST00000265686.8:c.1554+12G= MANE Select	ENSP00000265686.3:n.1554+12G=
ENST00000265686.7:c.1554+12G=	ENSP00000265686.3:n.1554+12G=
ENST00000525516.1:n.360G=
ENST00000525724.5:n.866+12G=
ENST00000528981.5:c.706+12G=
ENST00000532635.5:c.906+12G=	ENSP00000434407.1:n.906+12G=
ENST00000533005.5:n.667+12G=
NM_006019.3:c.1554+12G=	NP_006010.2:n.1554+12G=
NM_006053.3:c.906+12G=	NP_006044.1:n.906+12G=
XM_005273709.2:c.1554+12G=	XP_005273766.1:n.1554+12G=
XM_011544726.1:c.1554+12G=	XP_011543028.1:n.1554+12G=
XM_011544727.1:c.1554+12G=	XP_011543029.1:n.1554+12G=
XM_011544728.1:c.1554+12G=	XP_011543030.1:n.1554+12G=
XR_949754.1:n.1558+12G=
NM_001351059.1:c.660+12G=	NP_001337988.1:n.660+12G=
XM_024448320.1:c.1647+12G=	XP_024304088.1:n.1647+12G=
XM_024448321.1:c.1647+12G=	XP_024304089.1:n.1647+12G=
XM_024448322.1:c.1647+12G=	XP_024304090.1:n.1647+12G=
XM_024448323.1:c.1647+12G=	XP_024304091.1:n.1647+12G=
XM_024448324.1:c.1647+12G=	XP_024304092.1:n.1647+12G=
XR_001747721.2:n.1678+12G=
XR_001747722.1:n.1691+12G=
XR_001747723.2:n.1691+12G=
XR_002957115.1:n.1769+12G=
NM_006019.4:c.1554+12G= MANE Select	NP_006010.2:n.1554+12G=
NM_001351059.2:c.660+12G=	NP_001337988.1:n.660+12G=
NM_006053.4:c.906+12G=	NP_006044.1:n.906+12G=