Canonical Allele Identifier: CA6147127
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs113368668

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047860G>T , CM000673.2:g.68047860G>T GRCh38
NC_000011.9:g.67815327G>T , CM000673.1:g.67815327G>T GRCh37
NC_000011.8:g.67571903G>T NCBI36
NG_007878.1:g.13845G>T , LRG_115:g.13845G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.89-22G>T
ENST00000698254.1:c.993-22G>T ENSP00000513629.1:n.993-22G>T
ENST00000698255.1:c.1413-22G>T ENSP00000513630.1:n.1413-22G>T
ENST00000698256.1:c.930-22G>T
ENST00000698257.1:n.882-22G>T
ENST00000698258.1:n.577G>T
ENST00000698259.1:n.343G>T
ENST00000265686.8:c.1464-22G>T MANE Select ENSP00000265686.3:n.1464-22G>T
ENST00000265686.7:c.1464-22G>T ENSP00000265686.3:n.1464-22G>T
ENST00000525516.1:n.258-22G>T
ENST00000525724.5:n.776-22G>T
ENST00000528981.5:c.616-22G>T
ENST00000532635.5:c.816-22G>T ENSP00000434407.1:n.816-22G>T
ENST00000533005.5:n.555G>T
NM_006019.3:c.1464-22G>T NP_006010.2:n.1464-22G>T
NM_006053.3:c.816-22G>T NP_006044.1:n.816-22G>T
XM_005273709.2:c.1464-22G>T XP_005273766.1:n.1464-22G>T
XM_011544726.1:c.1464-22G>T XP_011543028.1:n.1464-22G>T
XM_011544727.1:c.1464-22G>T XP_011543029.1:n.1464-22G>T
XM_011544728.1:c.1464-22G>T XP_011543030.1:n.1464-22G>T
XM_011544729.1:c.1480-22G>T XP_011543031.1:n.1480-22G>T
XR_949754.1:n.1468-22G>T
NM_001351059.1:c.570-22G>T NP_001337988.1:n.570-22G>T
XM_024448320.1:c.1535G>T XP_024304088.1:p.Arg512Leu
XM_024448321.1:c.1535G>T XP_024304089.1:p.Arg512Leu
XM_024448322.1:c.1535G>T XP_024304090.1:p.Arg512Leu
XM_024448323.1:c.1535G>T XP_024304091.1:p.Arg512Leu
XM_024448324.1:c.1535G>T XP_024304092.1:p.Arg512Leu
XR_001747721.2:n.1588-22G>T
XR_001747722.1:n.1601-22G>T
XR_001747723.2:n.1601-22G>T
XR_002957115.1:n.1657G>T
NM_006019.4:c.1464-22G>T MANE Select NP_006010.2:n.1464-22G>T
NM_001351059.2:c.570-22G>T NP_001337988.1:n.570-22G>T
NM_006053.4:c.816-22G>T NP_006044.1:n.816-22G>T