Canonical Allele Identifier: CA381584336
Community Standard Title: NM_006019.4(TCIRG1):c.1460G>A (p.Trp487Ter)
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047801G>A , CM000673.2:g.68047801G>A GRCh38
NC_000011.9:g.67815268G>A , CM000673.1:g.67815268G>A GRCh37
NC_000011.8:g.67571844G>A NCBI36
NG_007878.1:g.13786G>A , LRG_115:g.13786G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.1460G>A MANE Select NP_006010.2:p.Trp487Ter
ENST00000265686.8:c.1460G>A MANE Select ENSP00000265686.3:p.Trp487Ter
NM_001351059.1:c.566G>A NP_001337988.1:p.Trp189Ter
NM_001351059.2:c.566G>A NP_001337988.1:p.Trp189Ter
NM_006019.3:c.1460G>A NP_006010.2:p.Trp487Ter
NM_006053.3:c.812G>A NP_006044.1:p.Trp271Ter
NM_006053.4:c.812G>A NP_006044.1:p.Trp271Ter
ENST00000265686.7:c.1460G>A ENSP00000265686.3:p.Trp487Ter
ENST00000525516.1:n.254G>A
ENST00000525724.5:n.772G>A
ENST00000528981.5:c.612G>A
ENST00000530449.2:n.85G>A
ENST00000532635.5:c.812G>A ENSP00000434407.1:p.Trp271Ter
ENST00000533005.5:n.496G>A
ENST00000698254.1:c.989G>A ENSP00000513629.1:p.Trp330Ter
ENST00000698255.1:c.1409G>A ENSP00000513630.1:p.Trp470Ter
ENST00000698256.1:c.926G>A
ENST00000698257.1:n.878G>A
ENST00000698258.1:n.518G>A
ENST00000698259.1:n.284G>A
XM_005273709.2:c.1460G>A XP_005273766.1:p.Trp487Ter
XM_011544726.1:c.1460G>A XP_011543028.1:p.Trp487Ter
XM_011544727.1:c.1460G>A XP_011543029.1:p.Trp487Ter
XM_011544728.1:c.1460G>A XP_011543030.1:p.Trp487Ter
XM_011544729.1:c.1476G>A XP_011543031.1:p.Leu492=
XM_024448320.1:c.1476G>A XP_024304088.1:p.Leu492=
XM_024448321.1:c.1476G>A XP_024304089.1:p.Leu492=
XM_024448322.1:c.1476G>A XP_024304090.1:p.Leu492=
XM_024448323.1:c.1476G>A XP_024304091.1:p.Leu492=
XM_024448324.1:c.1476G>A XP_024304092.1:p.Leu492=
XR_001747721.2:n.1584G>A
XR_001747722.1:n.1597G>A
XR_001747723.2:n.1597G>A
XR_002957115.1:n.1598G>A
XR_949754.1:n.1464G>A