Canonical Allele Identifier: CA6147346
Community Standard Title: NM_006019.4(TCIRG1):c.2008C>T (p.Arg670Ter)
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68049783C>T , CM000673.2:g.68049783C>T GRCh38
NC_000011.9:g.67817250C>T , CM000673.1:g.67817250C>T GRCh37
NC_000011.8:g.67573826C>T NCBI36
NG_007878.1:g.15768C>T , LRG_115:g.15768C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.2008C>T MANE Select NP_006010.2:p.Arg670Ter
ENST00000265686.8:c.2008C>T MANE Select ENSP00000265686.3:p.Arg670Ter
NM_001351059.1:c.1114C>T NP_001337988.1:p.Arg372Ter
NM_001351059.2:c.1114C>T NP_001337988.1:p.Arg372Ter
NM_006019.3:c.2008C>T NP_006010.2:p.Arg670Ter
NM_006053.3:c.1360C>T NP_006044.1:p.Arg454Ter
NM_006053.4:c.1360C>T NP_006044.1:p.Arg454Ter
ENST00000265686.7:c.2008C>T ENSP00000265686.3:p.Arg670Ter
ENST00000524870.1:n.636C>T
ENST00000525724.5:n.1320C>T
ENST00000530449.2:n.1001C>T
ENST00000532635.5:c.1360C>T ENSP00000434407.1:p.Arg454Ter
ENST00000533005.5:n.1121C>T
ENST00000698254.1:c.1537C>T ENSP00000513629.1:p.Arg513Ter
ENST00000698255.1:c.1957C>T ENSP00000513630.1:p.Arg653Ter
ENST00000698256.1:c.1474C>T
ENST00000698257.1:n.1426C>T
ENST00000698258.1:n.1143C>T
ENST00000698259.1:n.1277C>T
XM_005273709.2:c.2008C>T XP_005273766.1:p.Arg670Ter
XM_011544726.1:c.2008C>T XP_011543028.1:p.Arg670Ter
XM_011544727.1:c.2008C>T XP_011543029.1:p.Arg670Ter
XM_024448320.1:c.2101C>T XP_024304088.1:p.Arg701Ter
XM_024448321.1:c.2101C>T XP_024304089.1:p.Arg701Ter
XM_024448322.1:c.2101C>T XP_024304090.1:p.Arg701Ter
XM_024448323.1:c.2101C>T XP_024304091.1:p.Arg701Ter
XR_001747721.2:n.2177C>T
XR_001747722.1:n.2145C>T
XR_001747723.2:n.2190C>T
XR_002957115.1:n.2366C>T
XR_949754.1:n.2155C>T