Canonical Allele Identifier: CA1980428824
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047494C= , CM000673.2:g.68047494C= GRCh38
NC_000011.9:g.67814961C= , CM000673.1:g.67814961C= GRCh37
NC_000011.8:g.67571537C= NCBI36
NG_007878.1:g.13479C= , LRG_115:g.13479C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.756C= ENSP00000513629.1:p.His252=
ENST00000698255.1:c.1176C= ENSP00000513630.1:p.His392=
ENST00000698256.1:c.693C=
ENST00000698257.1:n.645C=
ENST00000698258.1:n.211C=
ENST00000698259.1:n.51C=
ENST00000265686.8:c.1227C= MANE Select ENSP00000265686.3:p.His409=
ENST00000265686.7:c.1227C= ENSP00000265686.3:p.His409=
ENST00000525516.1:n.21C=
ENST00000525724.5:n.539C=
ENST00000528981.5:c.379C=
ENST00000529364.1:c.638C=
ENST00000532635.5:c.579C= ENSP00000434407.1:p.His193=
ENST00000533005.5:n.263C=
NM_006019.3:c.1227C= NP_006010.2:p.His409=
NM_006053.3:c.579C= NP_006044.1:p.His193=
XM_005273709.2:c.1227C= XP_005273766.1:p.His409=
XM_011544726.1:c.1227C= XP_011543028.1:p.His409=
XM_011544727.1:c.1227C= XP_011543029.1:p.His409=
XM_011544728.1:c.1227C= XP_011543030.1:p.His409=
XM_011544729.1:c.1243C= XP_011543031.1:p.Arg415=
XR_949754.1:n.1231C=
NM_001351059.1:c.333C= NP_001337988.1:p.His111=
XM_024448320.1:c.1243C= XP_024304088.1:p.Arg415=
XM_024448321.1:c.1243C= XP_024304089.1:p.Arg415=
XM_024448322.1:c.1243C= XP_024304090.1:p.Arg415=
XM_024448323.1:c.1243C= XP_024304091.1:p.Arg415=
XM_024448324.1:c.1243C= XP_024304092.1:p.Arg415=
XR_001747721.2:n.1351C=
XR_001747722.1:n.1364C=
XR_001747723.2:n.1364C=
XR_002957115.1:n.1365C=
NM_006019.4:c.1227C= MANE Select NP_006010.2:p.His409=
NM_001351059.2:c.333C= NP_001337988.1:p.His111=
NM_006053.4:c.579C= NP_006044.1:p.His193=