Canonical Allele Identifier: CA381590633

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050224C>T , CM000673.2:g.68050224C>T	GRCh38
NC_000011.9:g.67817691C>T , CM000673.1:g.67817691C>T	GRCh37
NC_000011.8:g.67574267C>T	NCBI36
NG_007878.1:g.16209C>T , LRG_115:g.16209C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2206C>T MANE Select	NP_006010.2:p.Arg736Cys
ENST00000265686.8:c.2206C>T MANE Select	ENSP00000265686.3:p.Arg736Cys
NM_001351059.1:c.1312C>T	NP_001337988.1:p.Arg438Cys
NM_001351059.2:c.1312C>T	NP_001337988.1:p.Arg438Cys
NM_006019.3:c.2206C>T	NP_006010.2:p.Arg736Cys
NM_006053.3:c.1558C>T	NP_006044.1:p.Arg520Cys
NM_006053.4:c.1558C>T	NP_006044.1:p.Arg520Cys
ENST00000265686.7:c.2206C>T	ENSP00000265686.3:p.Arg736Cys
ENST00000525724.5:n.1518C>T
ENST00000530063.1:c.109C>T	ENSP00000432957.1:p.Arg37Cys
ENST00000530449.1:n.102C>T
ENST00000530449.2:n.1199C>T
ENST00000532635.5:c.1558C>T	ENSP00000434407.1:p.Arg520Cys
ENST00000533005.5:n.1319C>T
ENST00000698254.1:c.1735C>T	ENSP00000513629.1:p.Arg579Cys
ENST00000698255.1:c.2155C>T	ENSP00000513630.1:p.Arg719Cys
ENST00000698256.1:c.1672C>T
ENST00000698257.1:n.1624C>T
ENST00000698258.1:n.1341C>T
ENST00000698259.1:n.1475C>T
XM_005273709.2:c.2206C>T	XP_005273766.1:p.Arg736Cys
XM_011544726.1:c.2206C>T	XP_011543028.1:p.Arg736Cys
XM_011544727.1:c.2206C>T	XP_011543029.1:p.Arg736Cys
XM_024448320.1:c.2299C>T	XP_024304088.1:p.Arg767Cys
XM_024448321.1:c.2299C>T	XP_024304089.1:p.Arg767Cys
XM_024448322.1:c.2299C>T	XP_024304090.1:p.Arg767Cys
XM_024448323.1:c.2299C>T	XP_024304091.1:p.Arg767Cys
XR_001747721.2:n.2375C>T
XR_001747722.1:n.2343C>T
XR_001747723.2:n.2388C>T
XR_002957115.1:n.2564C>T
XR_949754.1:n.2353C>T