Canonical Allele Identifier: CA600238689
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1420485875

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048832A>T , CM000673.2:g.68048832A>T GRCh38
NC_000011.9:g.67816299A>T , CM000673.1:g.67816299A>T GRCh37
NC_000011.8:g.67572875A>T NCBI36
NG_007878.1:g.14817A>T , LRG_115:g.14817A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.180-47A>T
ENST00000698254.1:c.1084-47A>T ENSP00000513629.1:n.1084-47A>T
ENST00000698255.1:c.1504-47A>T ENSP00000513630.1:n.1504-47A>T
ENST00000698256.1:c.1021-47A>T
ENST00000698257.1:n.973-47A>T
ENST00000698258.1:n.690-47A>T
ENST00000698259.1:n.456-47A>T
ENST00000265686.8:c.1555-47A>T MANE Select ENSP00000265686.3:n.1555-47A>T
ENST00000265686.7:c.1555-47A>T ENSP00000265686.3:n.1555-47A>T
ENST00000525724.5:n.867-47A>T
ENST00000528981.5:c.707-47A>T
ENST00000532635.5:c.907-47A>T ENSP00000434407.1:n.907-47A>T
ENST00000533005.5:n.668-47A>T
NM_006019.3:c.1555-47A>T NP_006010.2:n.1555-47A>T
NM_006053.3:c.907-47A>T NP_006044.1:n.907-47A>T
XM_005273709.2:c.1555-47A>T XP_005273766.1:n.1555-47A>T
XM_011544726.1:c.1555-47A>T XP_011543028.1:n.1555-47A>T
XM_011544727.1:c.1555-47A>T XP_011543029.1:n.1555-47A>T
XM_011544728.1:c.1555-47A>T XP_011543030.1:n.1555-47A>T
XR_949754.1:n.1559-47A>T
NM_001351059.1:c.661-47A>T NP_001337988.1:n.661-47A>T
XM_024448320.1:c.1648-47A>T XP_024304088.1:n.1648-47A>T
XM_024448321.1:c.1648-47A>T XP_024304089.1:n.1648-47A>T
XM_024448322.1:c.1648-47A>T XP_024304090.1:n.1648-47A>T
XM_024448323.1:c.1648-47A>T XP_024304091.1:n.1648-47A>T
XM_024448324.1:c.1648-47A>T XP_024304092.1:n.1648-47A>T
XR_001747721.2:n.1679-47A>T
XR_001747722.1:n.1692-47A>T
XR_001747723.2:n.1692-47A>T
XR_002957115.1:n.1770-47A>T
NM_006019.4:c.1555-47A>T MANE Select NP_006010.2:n.1555-47A>T
NM_001351059.2:c.661-47A>T NP_001337988.1:n.661-47A>T
NM_006053.4:c.907-47A>T NP_006044.1:n.907-47A>T