Canonical Allele Identifier: CA6147061
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs780223256

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047614A>G , CM000673.2:g.68047614A>G GRCh38
NC_000011.9:g.67815081A>G , CM000673.1:g.67815081A>G GRCh37
NC_000011.8:g.67571657A>G NCBI36
NG_007878.1:g.13599A>G , LRG_115:g.13599A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.835-33A>G ENSP00000513629.1:n.835-33A>G
ENST00000698255.1:c.1255-33A>G ENSP00000513630.1:n.1255-33A>G
ENST00000698256.1:c.772-33A>G
ENST00000698257.1:n.724-33A>G
ENST00000698258.1:n.331A>G
ENST00000698259.1:n.130-33A>G
ENST00000265686.8:c.1306-33A>G MANE Select ENSP00000265686.3:n.1306-33A>G
ENST00000265686.7:c.1306-33A>G ENSP00000265686.3:n.1306-33A>G
ENST00000525516.1:n.100-33A>G
ENST00000525724.5:n.618-33A>G
ENST00000528981.5:c.458-33A>G
ENST00000529364.1:c.717-33A>G
ENST00000532635.5:c.658-33A>G ENSP00000434407.1:n.658-33A>G
ENST00000533005.5:n.342-33A>G
NM_006019.3:c.1306-33A>G NP_006010.2:n.1306-33A>G
NM_006053.3:c.658-33A>G NP_006044.1:n.658-33A>G
XM_005273709.2:c.1306-33A>G XP_005273766.1:n.1306-33A>G
XM_011544726.1:c.1306-33A>G XP_011543028.1:n.1306-33A>G
XM_011544727.1:c.1306-33A>G XP_011543029.1:n.1306-33A>G
XM_011544728.1:c.1306-33A>G XP_011543030.1:n.1306-33A>G
XM_011544729.1:c.1322-33A>G XP_011543031.1:n.1322-33A>G
XR_949754.1:n.1310-33A>G
NM_001351059.1:c.412-33A>G NP_001337988.1:n.412-33A>G
XM_024448320.1:c.1322-33A>G XP_024304088.1:n.1322-33A>G
XM_024448321.1:c.1322-33A>G XP_024304089.1:n.1322-33A>G
XM_024448322.1:c.1322-33A>G XP_024304090.1:n.1322-33A>G
XM_024448323.1:c.1322-33A>G XP_024304091.1:n.1322-33A>G
XM_024448324.1:c.1322-33A>G XP_024304092.1:n.1322-33A>G
XR_001747721.2:n.1430-33A>G
XR_001747722.1:n.1443-33A>G
XR_001747723.2:n.1443-33A>G
XR_002957115.1:n.1444-33A>G
NM_006019.4:c.1306-33A>G MANE Select NP_006010.2:n.1306-33A>G
NM_001351059.2:c.412-33A>G NP_001337988.1:n.412-33A>G
NM_006053.4:c.658-33A>G NP_006044.1:n.658-33A>G