Canonical Allele Identifier: CA1980429195

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047587_68047588delinsTG , CM000673.2:g.68047587_68047588delinsTG	GRCh38
NC_000011.9:g.67815054_67815055delinsTG , CM000673.1:g.67815054_67815055delinsTG	GRCh37
NC_000011.8:g.67571630_67571631delinsTG	NCBI36
NG_007878.1:g.13572_13573delinsTG , LRG_115:g.13572_13573delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.834+15_834+16delinsTG	ENSP00000513629.1:n.834+15_834+16delinsTG
ENST00000698255.1:c.1254+15_1254+16delinsTG	ENSP00000513630.1:n.1254+15_1254+16delinsTG
ENST00000698256.1:c.771+15_771+16delinsTG
ENST00000698257.1:n.723+15_723+16delinsTG
ENST00000698258.1:n.304_305delinsTG
ENST00000698259.1:n.129+15_129+16delinsTG
ENST00000265686.8:c.1305+15_1305+16delinsTG MANE Select	ENSP00000265686.3:n.1305+15_1305+16delinsTG
ENST00000265686.7:c.1305+15_1305+16delinsTG	ENSP00000265686.3:n.1305+15_1305+16delinsTG
ENST00000525516.1:n.99+15_99+16delinsTG
ENST00000525724.5:n.617+15_617+16delinsTG
ENST00000528981.5:c.457+15_457+16delinsTG
ENST00000529364.1:c.716+15_716+16delinsTG
ENST00000532635.5:c.657+15_657+16delinsTG	ENSP00000434407.1:n.657+15_657+16delinsTG
ENST00000533005.5:n.341+15_341+16delinsTG
NM_006019.3:c.1305+15_1305+16delinsTG	NP_006010.2:n.1305+15_1305+16delinsTG
NM_006053.3:c.657+15_657+16delinsTG	NP_006044.1:n.657+15_657+16delinsTG
XM_005273709.2:c.1305+15_1305+16delinsTG	XP_005273766.1:n.1305+15_1305+16delinsTG
XM_011544726.1:c.1305+15_1305+16delinsTG	XP_011543028.1:n.1305+15_1305+16delinsTG
XM_011544727.1:c.1305+15_1305+16delinsTG	XP_011543029.1:n.1305+15_1305+16delinsTG
XM_011544728.1:c.1305+15_1305+16delinsTG	XP_011543030.1:n.1305+15_1305+16delinsTG
XM_011544729.1:c.1321+15_1321+16delinsTG	XP_011543031.1:n.1321+15_1321+16delinsTG
XR_949754.1:n.1309+15_1309+16delinsTG
NM_001351059.1:c.411+15_411+16delinsTG	NP_001337988.1:n.411+15_411+16delinsTG
XM_024448320.1:c.1321+15_1321+16delinsTG	XP_024304088.1:n.1321+15_1321+16delinsTG
XM_024448321.1:c.1321+15_1321+16delinsTG	XP_024304089.1:n.1321+15_1321+16delinsTG
XM_024448322.1:c.1321+15_1321+16delinsTG	XP_024304090.1:n.1321+15_1321+16delinsTG
XM_024448323.1:c.1321+15_1321+16delinsTG	XP_024304091.1:n.1321+15_1321+16delinsTG
XM_024448324.1:c.1321+15_1321+16delinsTG	XP_024304092.1:n.1321+15_1321+16delinsTG
XR_001747721.2:n.1429+15_1429+16delinsTG
XR_001747722.1:n.1442+15_1442+16delinsTG
XR_001747723.2:n.1442+15_1442+16delinsTG
XR_002957115.1:n.1443+15_1443+16delinsTG
NM_006019.4:c.1305+15_1305+16delinsTG MANE Select	NP_006010.2:n.1305+15_1305+16delinsTG
NM_001351059.2:c.411+15_411+16delinsTG	NP_001337988.1:n.411+15_411+16delinsTG
NM_006053.4:c.657+15_657+16delinsTG	NP_006044.1:n.657+15_657+16delinsTG