Canonical Allele Identifier: CA939090197
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1855566709

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047585dup , CM000673.2:g.68047585dup GRCh38
NC_000011.9:g.67815052dup , CM000673.1:g.67815052dup GRCh37
NC_000011.8:g.67571628dup NCBI36
NG_007878.1:g.13570dup , LRG_115:g.13570dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.834+13dup ENSP00000513629.1:n.834+13dup
ENST00000698255.1:c.1254+13dup ENSP00000513630.1:n.1254+13dup
ENST00000698256.1:c.771+13dup
ENST00000698257.1:n.723+13dup
ENST00000698258.1:n.302dup
ENST00000698259.1:n.129+13dup
ENST00000265686.8:c.1305+13dup MANE Select ENSP00000265686.3:n.1305+13dup
ENST00000265686.7:c.1305+13dup ENSP00000265686.3:n.1305+13dup
ENST00000525516.1:n.99+13dup
ENST00000525724.5:n.617+13dup
ENST00000528981.5:c.457+13dup
ENST00000529364.1:c.716+13dup
ENST00000532635.5:c.657+13dup ENSP00000434407.1:n.657+13dup
ENST00000533005.5:n.341+13dup
NM_006019.3:c.1305+13dup NP_006010.2:n.1305+13dup
NM_006053.3:c.657+13dup NP_006044.1:n.657+13dup
XM_005273709.2:c.1305+13dup XP_005273766.1:n.1305+13dup
XM_011544726.1:c.1305+13dup XP_011543028.1:n.1305+13dup
XM_011544727.1:c.1305+13dup XP_011543029.1:n.1305+13dup
XM_011544728.1:c.1305+13dup XP_011543030.1:n.1305+13dup
XM_011544729.1:c.1321+13dup XP_011543031.1:n.1321+13dup
XR_949754.1:n.1309+13dup
NM_001351059.1:c.411+13dup NP_001337988.1:n.411+13dup
XM_024448320.1:c.1321+13dup XP_024304088.1:n.1321+13dup
XM_024448321.1:c.1321+13dup XP_024304089.1:n.1321+13dup
XM_024448322.1:c.1321+13dup XP_024304090.1:n.1321+13dup
XM_024448323.1:c.1321+13dup XP_024304091.1:n.1321+13dup
XM_024448324.1:c.1321+13dup XP_024304092.1:n.1321+13dup
XR_001747721.2:n.1429+13dup
XR_001747722.1:n.1442+13dup
XR_001747723.2:n.1442+13dup
XR_002957115.1:n.1443+13dup
NM_006019.4:c.1305+13dup MANE Select NP_006010.2:n.1305+13dup
NM_001351059.2:c.411+13dup NP_001337988.1:n.411+13dup
NM_006053.4:c.657+13dup NP_006044.1:n.657+13dup