Canonical Allele Identifier: CA1980430320

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048014T= , CM000673.2:g.68048014T=	GRCh38
NC_000011.9:g.67815481T= , CM000673.1:g.67815481T=	GRCh37
NC_000011.8:g.67572057T=	NCBI36
NG_007878.1:g.13999T= , LRG_115:g.13999T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.179+42T=
ENST00000698254.1:c.1083+42T=	ENSP00000513629.1:n.1083+42T=
ENST00000698255.1:c.1503+42T=	ENSP00000513630.1:n.1503+42T=
ENST00000698256.1:c.1020+42T=
ENST00000698257.1:n.972+42T=
ENST00000698258.1:n.689+42T=
ENST00000698259.1:n.455+42T=
ENST00000265686.8:c.1554+42T= MANE Select	ENSP00000265686.3:n.1554+42T=
ENST00000265686.7:c.1554+42T=	ENSP00000265686.3:n.1554+42T=
ENST00000525516.1:n.390T=
ENST00000525724.5:n.866+42T=
ENST00000528981.5:c.706+42T=
ENST00000532635.5:c.906+42T=	ENSP00000434407.1:n.906+42T=
ENST00000533005.5:n.667+42T=
NM_006019.3:c.1554+42T=	NP_006010.2:n.1554+42T=
NM_006053.3:c.906+42T=	NP_006044.1:n.906+42T=
XM_005273709.2:c.1554+42T=	XP_005273766.1:n.1554+42T=
XM_011544726.1:c.1554+42T=	XP_011543028.1:n.1554+42T=
XM_011544727.1:c.1554+42T=	XP_011543029.1:n.1554+42T=
XM_011544728.1:c.1554+42T=	XP_011543030.1:n.1554+42T=
XR_949754.1:n.1558+42T=
NM_001351059.1:c.660+42T=	NP_001337988.1:n.660+42T=
XM_024448320.1:c.1647+42T=	XP_024304088.1:n.1647+42T=
XM_024448321.1:c.1647+42T=	XP_024304089.1:n.1647+42T=
XM_024448322.1:c.1647+42T=	XP_024304090.1:n.1647+42T=
XM_024448323.1:c.1647+42T=	XP_024304091.1:n.1647+42T=
XM_024448324.1:c.1647+42T=	XP_024304092.1:n.1647+42T=
XR_001747721.2:n.1678+42T=
XR_001747722.1:n.1691+42T=
XR_001747723.2:n.1691+42T=
XR_002957115.1:n.1769+42T=
NM_006019.4:c.1554+42T= MANE Select	NP_006010.2:n.1554+42T=
NM_001351059.2:c.660+42T=	NP_001337988.1:n.660+42T=
NM_006053.4:c.906+42T=	NP_006044.1:n.906+42T=