Canonical Allele Identifier: CA2574899541

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047998_68047999insAAGGCAGTGGG , CM000673.2:g.68047998_68047999insAAGGCAGTGGG	GRCh38
NC_000011.9:g.67815465_67815466insAAGGCAGTGGG , CM000673.1:g.67815465_67815466insAAGGCAGTGGG	GRCh37
NC_000011.8:g.67572041_67572042insAAGGCAGTGGG	NCBI36
NG_007878.1:g.13983_13984insAAGGCAGTGGG , LRG_115:g.13983_13984insAAGGCAGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.179+26_179+27insAAGGCAGTGGG
ENST00000698254.1:c.1083+26_1083+27insAAGGCAGTGGG	ENSP00000513629.1:n.1083+26_1083+27insAAGGCAGTGGG
ENST00000698255.1:c.1503+26_1503+27insAAGGCAGTGGG	ENSP00000513630.1:n.1503+26_1503+27insAAGGCAGTGGG
ENST00000698256.1:c.1020+26_1020+27insAAGGCAGTGGG
ENST00000698257.1:n.972+26_972+27insAAGGCAGTGGG
ENST00000698258.1:n.689+26_689+27insAAGGCAGTGGG
ENST00000698259.1:n.455+26_455+27insAAGGCAGTGGG
ENST00000265686.8:c.1554+26_1554+27insAAGGCAGTGGG MANE Select	ENSP00000265686.3:n.1554+26_1554+27insAAGGCAGTGGG
ENST00000265686.7:c.1554+26_1554+27insAAGGCAGTGGG	ENSP00000265686.3:n.1554+26_1554+27insAAGGCAGTGGG
ENST00000525516.1:n.374_375insAAGGCAGTGGG
ENST00000525724.5:n.866+26_866+27insAAGGCAGTGGG
ENST00000528981.5:c.706+26_706+27insAAGGCAGTGGG
ENST00000532635.5:c.906+26_906+27insAAGGCAGTGGG	ENSP00000434407.1:n.906+26_906+27insAAGGCAGTGGG
ENST00000533005.5:n.667+26_667+27insAAGGCAGTGGG
NM_006019.3:c.1554+26_1554+27insAAGGCAGTGGG	NP_006010.2:n.1554+26_1554+27insAAGGCAGTGGG
NM_006053.3:c.906+26_906+27insAAGGCAGTGGG	NP_006044.1:n.906+26_906+27insAAGGCAGTGGG
XM_005273709.2:c.1554+26_1554+27insAAGGCAGTGGG	XP_005273766.1:n.1554+26_1554+27insAAGGCAGTGGG
XM_011544726.1:c.1554+26_1554+27insAAGGCAGTGGG	XP_011543028.1:n.1554+26_1554+27insAAGGCAGTGGG
XM_011544727.1:c.1554+26_1554+27insAAGGCAGTGGG	XP_011543029.1:n.1554+26_1554+27insAAGGCAGTGGG
XM_011544728.1:c.1554+26_1554+27insAAGGCAGTGGG	XP_011543030.1:n.1554+26_1554+27insAAGGCAGTGGG
XR_949754.1:n.1558+26_1558+27insAAGGCAGTGGG
NM_001351059.1:c.660+26_660+27insAAGGCAGTGGG	NP_001337988.1:n.660+26_660+27insAAGGCAGTGGG
XM_024448320.1:c.1647+26_1647+27insAAGGCAGTGGG	XP_024304088.1:n.1647+26_1647+27insAAGGCAGTGGG
XM_024448321.1:c.1647+26_1647+27insAAGGCAGTGGG	XP_024304089.1:n.1647+26_1647+27insAAGGCAGTGGG
XM_024448322.1:c.1647+26_1647+27insAAGGCAGTGGG	XP_024304090.1:n.1647+26_1647+27insAAGGCAGTGGG
XM_024448323.1:c.1647+26_1647+27insAAGGCAGTGGG	XP_024304091.1:n.1647+26_1647+27insAAGGCAGTGGG
XM_024448324.1:c.1647+26_1647+27insAAGGCAGTGGG	XP_024304092.1:n.1647+26_1647+27insAAGGCAGTGGG
XR_001747721.2:n.1678+26_1678+27insAAGGCAGTGGG
XR_001747722.1:n.1691+26_1691+27insAAGGCAGTGGG
XR_001747723.2:n.1691+26_1691+27insAAGGCAGTGGG
XR_002957115.1:n.1769+26_1769+27insAAGGCAGTGGG
NM_006019.4:c.1554+26_1554+27insAAGGCAGTGGG MANE Select	NP_006010.2:n.1554+26_1554+27insAAGGCAGTGGG
NM_001351059.2:c.660+26_660+27insAAGGCAGTGGG	NP_001337988.1:n.660+26_660+27insAAGGCAGTGGG
NM_006053.4:c.906+26_906+27insAAGGCAGTGGG	NP_006044.1:n.906+26_906+27insAAGGCAGTGGG