Canonical Allele Identifier: CA6146858

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044303C>T , CM000673.2:g.68044303C>T	GRCh38
NC_000011.9:g.67811770C>T , CM000673.1:g.67811770C>T	GRCh37
NC_000011.8:g.67568346C>T	NCBI36
NG_007878.1:g.10288C>T , LRG_115:g.10288C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.979C>T MANE Select	NP_006010.2:p.Arg327Ter
ENST00000265686.8:c.979C>T MANE Select	ENSP00000265686.3:p.Arg327Ter
NM_001351059.1:c.85C>T	NP_001337988.1:p.Arg29Ter
NM_001351059.2:c.85C>T	NP_001337988.1:p.Arg29Ter
NM_006019.3:c.979C>T	NP_006010.2:p.Arg327Ter
NM_006053.3:c.331C>T	NP_006044.1:p.Arg111Ter
NM_006053.4:c.331C>T	NP_006044.1:p.Arg111Ter
ENST00000265686.7:c.979C>T	ENSP00000265686.3:p.Arg327Ter
ENST00000525724.5:n.291C>T
ENST00000528981.5:c.69C>T
ENST00000529364.1:c.479C>T
ENST00000532635.5:c.331C>T	ENSP00000434407.1:p.Arg111Ter
ENST00000533005.5:n.15C>T
ENST00000698254.1:c.508C>T	ENSP00000513629.1:p.Arg170Ter
ENST00000698255.1:c.928C>T	ENSP00000513630.1:p.Arg310Ter
ENST00000698256.1:c.445C>T
ENST00000698257.1:n.397C>T
XM_005273709.2:c.979C>T	XP_005273766.1:p.Arg327Ter
XM_011544726.1:c.979C>T	XP_011543028.1:p.Arg327Ter
XM_011544727.1:c.979C>T	XP_011543029.1:p.Arg327Ter
XM_011544728.1:c.979C>T	XP_011543030.1:p.Arg327Ter
XM_011544729.1:c.995C>T	XP_011543031.1:p.Ala332Val
XM_024448320.1:c.995C>T	XP_024304088.1:p.Ala332Val
XM_024448321.1:c.995C>T	XP_024304089.1:p.Ala332Val
XM_024448322.1:c.995C>T	XP_024304090.1:p.Ala332Val
XM_024448323.1:c.995C>T	XP_024304091.1:p.Ala332Val
XM_024448324.1:c.995C>T	XP_024304092.1:p.Ala332Val
XR_001747721.2:n.1103C>T
XR_001747722.1:n.1116C>T
XR_001747723.2:n.1116C>T
XR_002957115.1:n.1117C>T
XR_949754.1:n.983C>T