Canonical Allele Identifier: CA6147091
Community Standard Title: NM_006019.4(TCIRG1):c.1387G>T (p.Glu463Ter)
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047728G>T , CM000673.2:g.68047728G>T GRCh38
NC_000011.9:g.67815195G>T , CM000673.1:g.67815195G>T GRCh37
NC_000011.8:g.67571771G>T NCBI36
NG_007878.1:g.13713G>T , LRG_115:g.13713G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006019.4:c.1387G>T MANE Select NP_006010.2:p.Glu463Ter
ENST00000265686.8:c.1387G>T MANE Select ENSP00000265686.3:p.Glu463Ter
NM_001351059.1:c.493G>T NP_001337988.1:p.Glu165Ter
NM_001351059.2:c.493G>T NP_001337988.1:p.Glu165Ter
NM_006019.3:c.1387G>T NP_006010.2:p.Glu463Ter
NM_006053.3:c.739G>T NP_006044.1:p.Glu247Ter
NM_006053.4:c.739G>T NP_006044.1:p.Glu247Ter
ENST00000265686.7:c.1387G>T ENSP00000265686.3:p.Glu463Ter
ENST00000525516.1:n.181G>T
ENST00000525724.5:n.699G>T
ENST00000528981.5:c.539G>T
ENST00000529364.1:c.798G>T
ENST00000530449.2:n.12G>T
ENST00000532635.5:c.739G>T ENSP00000434407.1:p.Glu247Ter
ENST00000533005.5:n.423G>T
ENST00000698254.1:c.916G>T ENSP00000513629.1:p.Glu306Ter
ENST00000698255.1:c.1336G>T ENSP00000513630.1:p.Glu446Ter
ENST00000698256.1:c.853G>T
ENST00000698257.1:n.805G>T
ENST00000698258.1:n.445G>T
ENST00000698259.1:n.211G>T
XM_005273709.2:c.1387G>T XP_005273766.1:p.Glu463Ter
XM_011544726.1:c.1387G>T XP_011543028.1:p.Glu463Ter
XM_011544727.1:c.1387G>T XP_011543029.1:p.Glu463Ter
XM_011544728.1:c.1387G>T XP_011543030.1:p.Glu463Ter
XM_011544729.1:c.1403G>T XP_011543031.1:p.Arg468Leu
XM_024448320.1:c.1403G>T XP_024304088.1:p.Arg468Leu
XM_024448321.1:c.1403G>T XP_024304089.1:p.Arg468Leu
XM_024448322.1:c.1403G>T XP_024304090.1:p.Arg468Leu
XM_024448323.1:c.1403G>T XP_024304091.1:p.Arg468Leu
XM_024448324.1:c.1403G>T XP_024304092.1:p.Arg468Leu
XR_001747721.2:n.1511G>T
XR_001747722.1:n.1524G>T
XR_001747723.2:n.1524G>T
XR_002957115.1:n.1525G>T
XR_949754.1:n.1391G>T