Canonical Allele Identifier: CA381585039
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1263166960

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048913T>C , CM000673.2:g.68048913T>C GRCh38
NC_000011.9:g.67816380T>C , CM000673.1:g.67816380T>C GRCh37
NC_000011.8:g.67572956T>C NCBI36
NG_007878.1:g.14898T>C , LRG_115:g.14898T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.214T>C
ENST00000698254.1:c.1118T>C ENSP00000513629.1:p.Leu373Pro
ENST00000698255.1:c.1538T>C ENSP00000513630.1:p.Leu513Pro
ENST00000698256.1:c.1055T>C
ENST00000698257.1:n.1007T>C
ENST00000698258.1:n.724T>C
ENST00000698259.1:n.490T>C
ENST00000265686.8:c.1589T>C MANE Select ENSP00000265686.3:p.Leu530Pro
ENST00000265686.7:c.1589T>C ENSP00000265686.3:p.Leu530Pro
ENST00000525724.5:n.901T>C
ENST00000528981.5:c.741T>C
ENST00000532635.5:c.941T>C ENSP00000434407.1:p.Leu314Pro
ENST00000533005.5:n.702T>C
NM_006019.3:c.1589T>C NP_006010.2:p.Leu530Pro
NM_006053.3:c.941T>C NP_006044.1:p.Leu314Pro
XM_005273709.2:c.1589T>C XP_005273766.1:p.Leu530Pro
XM_011544726.1:c.1589T>C XP_011543028.1:p.Leu530Pro
XM_011544727.1:c.1589T>C XP_011543029.1:p.Leu530Pro
XM_011544728.1:c.1589T>C XP_011543030.1:p.Leu530Pro
XR_949754.1:n.1593T>C
NM_001351059.1:c.695T>C NP_001337988.1:p.Leu232Pro
XM_024448320.1:c.1682T>C XP_024304088.1:p.Leu561Pro
XM_024448321.1:c.1682T>C XP_024304089.1:p.Leu561Pro
XM_024448322.1:c.1682T>C XP_024304090.1:p.Leu561Pro
XM_024448323.1:c.1682T>C XP_024304091.1:p.Leu561Pro
XM_024448324.1:c.1682T>C XP_024304092.1:p.Leu561Pro
XR_001747721.2:n.1713T>C
XR_001747722.1:n.1726T>C
XR_001747723.2:n.1726T>C
XR_002957115.1:n.1804T>C
NM_006019.4:c.1589T>C MANE Select NP_006010.2:p.Leu530Pro
NM_001351059.2:c.695T>C NP_001337988.1:p.Leu232Pro
NM_006053.4:c.941T>C NP_006044.1:p.Leu314Pro