Canonical Allele Identifier: CA381583819
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047707T>G , CM000673.2:g.68047707T>G GRCh38
NC_000011.9:g.67815174T>G , CM000673.1:g.67815174T>G GRCh37
NC_000011.8:g.67571750T>G NCBI36
NG_007878.1:g.13692T>G , LRG_115:g.13692T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.895T>G ENSP00000513629.1:p.Tyr299Asp
ENST00000698255.1:c.1315T>G ENSP00000513630.1:p.Tyr439Asp
ENST00000698256.1:c.832T>G
ENST00000698257.1:n.784T>G
ENST00000698258.1:n.424T>G
ENST00000698259.1:n.190T>G
ENST00000265686.8:c.1366T>G MANE Select ENSP00000265686.3:p.Tyr456Asp
ENST00000265686.7:c.1366T>G ENSP00000265686.3:p.Tyr456Asp
ENST00000525516.1:n.160T>G
ENST00000525724.5:n.678T>G
ENST00000528981.5:c.518T>G
ENST00000529364.1:c.777T>G
ENST00000532635.5:c.718T>G ENSP00000434407.1:p.Tyr240Asp
ENST00000533005.5:n.402T>G
NM_006019.3:c.1366T>G NP_006010.2:p.Tyr456Asp
NM_006053.3:c.718T>G NP_006044.1:p.Tyr240Asp
XM_005273709.2:c.1366T>G XP_005273766.1:p.Tyr456Asp
XM_011544726.1:c.1366T>G XP_011543028.1:p.Tyr456Asp
XM_011544727.1:c.1366T>G XP_011543029.1:p.Tyr456Asp
XM_011544728.1:c.1366T>G XP_011543030.1:p.Tyr456Asp
XM_011544729.1:c.1382T>G XP_011543031.1:p.Leu461Arg
XR_949754.1:n.1370T>G
NM_001351059.1:c.472T>G NP_001337988.1:p.Tyr158Asp
XM_024448320.1:c.1382T>G XP_024304088.1:p.Leu461Arg
XM_024448321.1:c.1382T>G XP_024304089.1:p.Leu461Arg
XM_024448322.1:c.1382T>G XP_024304090.1:p.Leu461Arg
XM_024448323.1:c.1382T>G XP_024304091.1:p.Leu461Arg
XM_024448324.1:c.1382T>G XP_024304092.1:p.Leu461Arg
XR_001747721.2:n.1490T>G
XR_001747722.1:n.1503T>G
XR_001747723.2:n.1503T>G
XR_002957115.1:n.1504T>G
NM_006019.4:c.1366T>G MANE Select NP_006010.2:p.Tyr456Asp
NM_001351059.2:c.472T>G NP_001337988.1:p.Tyr158Asp
NM_006053.4:c.718T>G NP_006044.1:p.Tyr240Asp