Canonical Allele Identifier: CA2574899523

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047781del , CM000673.2:g.68047781del	GRCh38
NC_000011.9:g.67815248del , CM000673.1:g.67815248del	GRCh37
NC_000011.8:g.67571824del	NCBI36
NG_007878.1:g.13766del , LRG_115:g.13766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.65del
ENST00000698254.1:c.969del	ENSP00000513629.1:p.Met324TrpfsTer?
ENST00000698255.1:c.1389del	ENSP00000513630.1:p.Met464TrpfsTer?
ENST00000698256.1:c.906del
ENST00000698257.1:n.858del
ENST00000698258.1:n.498del
ENST00000698259.1:n.264del
ENST00000265686.8:c.1440del MANE Select	ENSP00000265686.3:p.Met481TrpfsTer?
ENST00000265686.7:c.1440del	ENSP00000265686.3:p.Met481TrpfsTer?
ENST00000525516.1:n.234del
ENST00000525724.5:n.752del
ENST00000528981.5:c.592del
ENST00000529364.1:c.851del
ENST00000532635.5:c.792del	ENSP00000434407.1:p.Met265TrpfsTer?
ENST00000533005.5:n.476del
NM_006019.3:c.1440del	NP_006010.2:p.Met481TrpfsTer?
NM_006053.3:c.792del	NP_006044.1:p.Met265TrpfsTer?
XM_005273709.2:c.1440del	XP_005273766.1:p.Met481TrpfsTer?
XM_011544726.1:c.1440del	XP_011543028.1:p.Met481TrpfsTer?
XM_011544727.1:c.1440del	XP_011543029.1:p.Met481TrpfsTer?
XM_011544728.1:c.1440del	XP_011543030.1:p.Met481TrpfsTer?
XM_011544729.1:c.1456del	XP_011543031.1:p.His486MetfsTer?
XR_949754.1:n.1444del
NM_001351059.1:c.546del	NP_001337988.1:p.Met183TrpfsTer?
XM_024448320.1:c.1456del	XP_024304088.1:p.His486MetfsTer9
XM_024448321.1:c.1456del	XP_024304089.1:p.His486MetfsTer9
XM_024448322.1:c.1456del	XP_024304090.1:p.His486MetfsTer9
XM_024448323.1:c.1456del	XP_024304091.1:p.His486MetfsTer9
XM_024448324.1:c.1456del	XP_024304092.1:p.His486MetfsTer9
XR_001747721.2:n.1564del
XR_001747722.1:n.1577del
XR_001747723.2:n.1577del
XR_002957115.1:n.1578del
NM_006019.4:c.1440del MANE Select	NP_006010.2:p.Met481TrpfsTer?
NM_001351059.2:c.546del	NP_001337988.1:p.Met183TrpfsTer?
NM_006053.4:c.792del	NP_006044.1:p.Met265TrpfsTer?