Canonical Allele Identifier: CA1980430277

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047992_68047993delinsGT , CM000673.2:g.68047992_68047993delinsGT	GRCh38
NC_000011.9:g.67815459_67815460delinsGT , CM000673.1:g.67815459_67815460delinsGT	GRCh37
NC_000011.8:g.67572035_67572036delinsGT	NCBI36
NG_007878.1:g.13977_13978delinsGT , LRG_115:g.13977_13978delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.179+20_179+21delinsGT
ENST00000698254.1:c.1083+20_1083+21delinsGT	ENSP00000513629.1:n.1083+20_1083+21delinsGT
ENST00000698255.1:c.1503+20_1503+21delinsGT	ENSP00000513630.1:n.1503+20_1503+21delinsGT
ENST00000698256.1:c.1020+20_1020+21delinsGT
ENST00000698257.1:n.972+20_972+21delinsGT
ENST00000698258.1:n.689+20_689+21delinsGT
ENST00000698259.1:n.455+20_455+21delinsGT
ENST00000265686.8:c.1554+20_1554+21delinsGT MANE Select	ENSP00000265686.3:n.1554+20_1554+21delinsGT
ENST00000265686.7:c.1554+20_1554+21delinsGT	ENSP00000265686.3:n.1554+20_1554+21delinsGT
ENST00000525516.1:n.368_369delinsGT
ENST00000525724.5:n.866+20_866+21delinsGT
ENST00000528981.5:c.706+20_706+21delinsGT
ENST00000532635.5:c.906+20_906+21delinsGT	ENSP00000434407.1:n.906+20_906+21delinsGT
ENST00000533005.5:n.667+20_667+21delinsGT
NM_006019.3:c.1554+20_1554+21delinsGT	NP_006010.2:n.1554+20_1554+21delinsGT
NM_006053.3:c.906+20_906+21delinsGT	NP_006044.1:n.906+20_906+21delinsGT
XM_005273709.2:c.1554+20_1554+21delinsGT	XP_005273766.1:n.1554+20_1554+21delinsGT
XM_011544726.1:c.1554+20_1554+21delinsGT	XP_011543028.1:n.1554+20_1554+21delinsGT
XM_011544727.1:c.1554+20_1554+21delinsGT	XP_011543029.1:n.1554+20_1554+21delinsGT
XM_011544728.1:c.1554+20_1554+21delinsGT	XP_011543030.1:n.1554+20_1554+21delinsGT
XR_949754.1:n.1558+20_1558+21delinsGT
NM_001351059.1:c.660+20_660+21delinsGT	NP_001337988.1:n.660+20_660+21delinsGT
XM_024448320.1:c.1647+20_1647+21delinsGT	XP_024304088.1:n.1647+20_1647+21delinsGT
XM_024448321.1:c.1647+20_1647+21delinsGT	XP_024304089.1:n.1647+20_1647+21delinsGT
XM_024448322.1:c.1647+20_1647+21delinsGT	XP_024304090.1:n.1647+20_1647+21delinsGT
XM_024448323.1:c.1647+20_1647+21delinsGT	XP_024304091.1:n.1647+20_1647+21delinsGT
XM_024448324.1:c.1647+20_1647+21delinsGT	XP_024304092.1:n.1647+20_1647+21delinsGT
XR_001747721.2:n.1678+20_1678+21delinsGT
XR_001747722.1:n.1691+20_1691+21delinsGT
XR_001747723.2:n.1691+20_1691+21delinsGT
XR_002957115.1:n.1769+20_1769+21delinsGT
NM_006019.4:c.1554+20_1554+21delinsGT MANE Select	NP_006010.2:n.1554+20_1554+21delinsGT
NM_001351059.2:c.660+20_660+21delinsGT	NP_001337988.1:n.660+20_660+21delinsGT
NM_006053.4:c.906+20_906+21delinsGT	NP_006044.1:n.906+20_906+21delinsGT