Canonical Allele Identifier: CA381587555

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68049292C>T , CM000673.2:g.68049292C>T	GRCh38
NC_000011.9:g.67816759C>T , CM000673.1:g.67816759C>T	GRCh37
NC_000011.8:g.67573335C>T	NCBI36
NG_007878.1:g.15277C>T , LRG_115:g.15277C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1885C>T MANE Select	NP_006010.2:p.Gln629Ter
ENST00000265686.8:c.1885C>T MANE Select	ENSP00000265686.3:p.Gln629Ter
NM_001351059.1:c.991C>T	NP_001337988.1:p.Gln331Ter
NM_001351059.2:c.991C>T	NP_001337988.1:p.Gln331Ter
NM_006019.3:c.1885C>T	NP_006010.2:p.Gln629Ter
NM_006053.3:c.1237C>T	NP_006044.1:p.Gln413Ter
NM_006053.4:c.1237C>T	NP_006044.1:p.Gln413Ter
ENST00000265686.7:c.1885C>T	ENSP00000265686.3:p.Gln629Ter
ENST00000524870.1:n.145C>T
ENST00000525724.5:n.1197C>T
ENST00000530449.2:n.510C>T
ENST00000532635.5:c.1237C>T	ENSP00000434407.1:p.Gln413Ter
ENST00000533005.5:n.998C>T
ENST00000698254.1:c.1414C>T	ENSP00000513629.1:p.Gln472Ter
ENST00000698255.1:c.1834C>T	ENSP00000513630.1:p.Gln612Ter
ENST00000698256.1:c.1351C>T
ENST00000698257.1:n.1303C>T
ENST00000698258.1:n.1020C>T
ENST00000698259.1:n.786C>T
XM_005273709.2:c.1885C>T	XP_005273766.1:p.Gln629Ter
XM_011544726.1:c.1885C>T	XP_011543028.1:p.Gln629Ter
XM_011544727.1:c.1885C>T	XP_011543029.1:p.Gln629Ter
XM_011544728.1:c.1885C>T	XP_011543030.1:p.Gln629Ter
XM_024448320.1:c.1978C>T	XP_024304088.1:p.Gln660Ter
XM_024448321.1:c.1978C>T	XP_024304089.1:p.Gln660Ter
XM_024448322.1:c.1978C>T	XP_024304090.1:p.Gln660Ter
XM_024448323.1:c.1978C>T	XP_024304091.1:p.Gln660Ter
XM_024448324.1:c.1978C>T	XP_024304092.1:p.Gln660Ter
XR_001747721.2:n.2009C>T
XR_001747722.1:n.2022C>T
XR_001747723.2:n.2022C>T
XR_002957115.1:n.2100C>T
XR_949754.1:n.1889C>T