Canonical Allele Identifier: CA381584065
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047753T>A , CM000673.2:g.68047753T>A GRCh38
NC_000011.9:g.67815220T>A , CM000673.1:g.67815220T>A GRCh37
NC_000011.8:g.67571796T>A NCBI36
NG_007878.1:g.13738T>A , LRG_115:g.13738T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.37T>A
ENST00000698254.1:c.941T>A ENSP00000513629.1:p.Ile314Asn
ENST00000698255.1:c.1361T>A ENSP00000513630.1:p.Ile454Asn
ENST00000698256.1:c.878T>A
ENST00000698257.1:n.830T>A
ENST00000698258.1:n.470T>A
ENST00000698259.1:n.236T>A
ENST00000265686.8:c.1412T>A MANE Select ENSP00000265686.3:p.Ile471Asn
ENST00000265686.7:c.1412T>A ENSP00000265686.3:p.Ile471Asn
ENST00000525516.1:n.206T>A
ENST00000525724.5:n.724T>A
ENST00000528981.5:c.564T>A
ENST00000529364.1:c.823T>A
ENST00000532635.5:c.764T>A ENSP00000434407.1:p.Ile255Asn
ENST00000533005.5:n.448T>A
NM_006019.3:c.1412T>A NP_006010.2:p.Ile471Asn
NM_006053.3:c.764T>A NP_006044.1:p.Ile255Asn
XM_005273709.2:c.1412T>A XP_005273766.1:p.Ile471Asn
XM_011544726.1:c.1412T>A XP_011543028.1:p.Ile471Asn
XM_011544727.1:c.1412T>A XP_011543029.1:p.Ile471Asn
XM_011544728.1:c.1412T>A XP_011543030.1:p.Ile471Asn
XM_011544729.1:c.1428T>A XP_011543031.1:p.His476Gln
XR_949754.1:n.1416T>A
NM_001351059.1:c.518T>A NP_001337988.1:p.Ile173Asn
XM_024448320.1:c.1428T>A XP_024304088.1:p.His476Gln
XM_024448321.1:c.1428T>A XP_024304089.1:p.His476Gln
XM_024448322.1:c.1428T>A XP_024304090.1:p.His476Gln
XM_024448323.1:c.1428T>A XP_024304091.1:p.His476Gln
XM_024448324.1:c.1428T>A XP_024304092.1:p.His476Gln
XR_001747721.2:n.1536T>A
XR_001747722.1:n.1549T>A
XR_001747723.2:n.1549T>A
XR_002957115.1:n.1550T>A
NM_006019.4:c.1412T>A MANE Select NP_006010.2:p.Ile471Asn
NM_001351059.2:c.518T>A NP_001337988.1:p.Ile173Asn
NM_006053.4:c.764T>A NP_006044.1:p.Ile255Asn