Canonical Allele Identifier: CA381589473

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050014G>A , CM000673.2:g.68050014G>A	GRCh38
NC_000011.9:g.67817481G>A , CM000673.1:g.67817481G>A	GRCh37
NC_000011.8:g.67574057G>A	NCBI36
NG_007878.1:g.15999G>A , LRG_115:g.15999G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2066G>A MANE Select	NP_006010.2:p.Trp689Ter
ENST00000265686.8:c.2066G>A MANE Select	ENSP00000265686.3:p.Trp689Ter
NM_001351059.1:c.1172G>A	NP_001337988.1:p.Trp391Ter
NM_001351059.2:c.1172G>A	NP_001337988.1:p.Trp391Ter
NM_006019.3:c.2066G>A	NP_006010.2:p.Trp689Ter
NM_006053.3:c.1418G>A	NP_006044.1:p.Trp473Ter
NM_006053.4:c.1418G>A	NP_006044.1:p.Trp473Ter
ENST00000265686.7:c.2066G>A	ENSP00000265686.3:p.Trp689Ter
ENST00000524870.1:n.694G>A
ENST00000525724.5:n.1378G>A
ENST00000530449.2:n.1059G>A
ENST00000532635.5:c.1418G>A	ENSP00000434407.1:p.Trp473Ter
ENST00000533005.5:n.1179G>A
ENST00000698254.1:c.1595G>A	ENSP00000513629.1:p.Trp532Ter
ENST00000698255.1:c.2015G>A	ENSP00000513630.1:p.Trp672Ter
ENST00000698256.1:c.1532G>A
ENST00000698257.1:n.1484G>A
ENST00000698258.1:n.1201G>A
ENST00000698259.1:n.1335G>A
XM_005273709.2:c.2066G>A	XP_005273766.1:p.Trp689Ter
XM_011544726.1:c.2066G>A	XP_011543028.1:p.Trp689Ter
XM_011544727.1:c.2066G>A	XP_011543029.1:p.Trp689Ter
XM_024448320.1:c.2159G>A	XP_024304088.1:p.Trp720Ter
XM_024448321.1:c.2159G>A	XP_024304089.1:p.Trp720Ter
XM_024448322.1:c.2159G>A	XP_024304090.1:p.Trp720Ter
XM_024448323.1:c.2159G>A	XP_024304091.1:p.Trp720Ter
XR_001747721.2:n.2235G>A
XR_001747722.1:n.2203G>A
XR_001747723.2:n.2248G>A
XR_002957115.1:n.2424G>A
XR_949754.1:n.2213G>A