Canonical Allele Identifier: CA381583872
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047718C>A , CM000673.2:g.68047718C>A GRCh38
NC_000011.9:g.67815185C>A , CM000673.1:g.67815185C>A GRCh37
NC_000011.8:g.67571761C>A NCBI36
NG_007878.1:g.13703C>A , LRG_115:g.13703C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.2C>A
ENST00000698254.1:c.906C>A ENSP00000513629.1:p.Phe302Leu
ENST00000698255.1:c.1326C>A ENSP00000513630.1:p.Phe442Leu
ENST00000698256.1:c.843C>A
ENST00000698257.1:n.795C>A
ENST00000698258.1:n.435C>A
ENST00000698259.1:n.201C>A
ENST00000265686.8:c.1377C>A MANE Select ENSP00000265686.3:p.Phe459Leu
ENST00000265686.7:c.1377C>A ENSP00000265686.3:p.Phe459Leu
ENST00000525516.1:n.171C>A
ENST00000525724.5:n.689C>A
ENST00000528981.5:c.529C>A
ENST00000529364.1:c.788C>A
ENST00000532635.5:c.729C>A ENSP00000434407.1:p.Phe243Leu
ENST00000533005.5:n.413C>A
NM_006019.3:c.1377C>A NP_006010.2:p.Phe459Leu
NM_006053.3:c.729C>A NP_006044.1:p.Phe243Leu
XM_005273709.2:c.1377C>A XP_005273766.1:p.Phe459Leu
XM_011544726.1:c.1377C>A XP_011543028.1:p.Phe459Leu
XM_011544727.1:c.1377C>A XP_011543029.1:p.Phe459Leu
XM_011544728.1:c.1377C>A XP_011543030.1:p.Phe459Leu
XM_011544729.1:c.1393C>A XP_011543031.1:p.His465Asn
XR_949754.1:n.1381C>A
NM_001351059.1:c.483C>A NP_001337988.1:p.Phe161Leu
XM_024448320.1:c.1393C>A XP_024304088.1:p.His465Asn
XM_024448321.1:c.1393C>A XP_024304089.1:p.His465Asn
XM_024448322.1:c.1393C>A XP_024304090.1:p.His465Asn
XM_024448323.1:c.1393C>A XP_024304091.1:p.His465Asn
XM_024448324.1:c.1393C>A XP_024304092.1:p.His465Asn
XR_001747721.2:n.1501C>A
XR_001747722.1:n.1514C>A
XR_001747723.2:n.1514C>A
XR_002957115.1:n.1515C>A
NM_006019.4:c.1377C>A MANE Select NP_006010.2:p.Phe459Leu
NM_001351059.2:c.483C>A NP_001337988.1:p.Phe161Leu
NM_006053.4:c.729C>A NP_006044.1:p.Phe243Leu