Canonical Allele Identifier: CA475514073

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815209C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047742C>G , CM000673.2:g.68047742C>G	GRCh38
NC_000011.9:g.67815209C>G , CM000673.1:g.67815209C>G	GRCh37
NC_000011.8:g.67571785C>G	NCBI36
NG_007878.1:g.13727C>G , LRG_115:g.13727C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.26C>G
ENST00000698254.1:c.930C>G	ENSP00000513629.1:p.Arg310=
ENST00000698255.1:c.1350C>G	ENSP00000513630.1:p.Arg450=
ENST00000698256.1:c.867C>G
ENST00000698257.1:n.819C>G
ENST00000698258.1:n.459C>G
ENST00000698259.1:n.225C>G
ENST00000265686.8:c.1401C>G MANE Select	ENSP00000265686.3:p.Arg467=
ENST00000265686.7:c.1401C>G	ENSP00000265686.3:p.Arg467=
ENST00000525516.1:n.195C>G
ENST00000525724.5:n.713C>G
ENST00000528981.5:c.553C>G
ENST00000529364.1:c.812C>G
ENST00000532635.5:c.753C>G	ENSP00000434407.1:p.Arg251=
ENST00000533005.5:n.437C>G
NM_006019.3:c.1401C>G	NP_006010.2:p.Arg467=
NM_006053.3:c.753C>G	NP_006044.1:p.Arg251=
XM_005273709.2:c.1401C>G	XP_005273766.1:p.Arg467=
XM_011544726.1:c.1401C>G	XP_011543028.1:p.Arg467=
XM_011544727.1:c.1401C>G	XP_011543029.1:p.Arg467=
XM_011544728.1:c.1401C>G	XP_011543030.1:p.Arg467=
XM_011544729.1:c.1417C>G	XP_011543031.1:p.Arg473Gly
XR_949754.1:n.1405C>G
NM_001351059.1:c.507C>G	NP_001337988.1:p.Arg169=
XM_024448320.1:c.1417C>G	XP_024304088.1:p.Arg473Gly
XM_024448321.1:c.1417C>G	XP_024304089.1:p.Arg473Gly
XM_024448322.1:c.1417C>G	XP_024304090.1:p.Arg473Gly
XM_024448323.1:c.1417C>G	XP_024304091.1:p.Arg473Gly
XM_024448324.1:c.1417C>G	XP_024304092.1:p.Arg473Gly
XR_001747721.2:n.1525C>G
XR_001747722.1:n.1538C>G
XR_001747723.2:n.1538C>G
XR_002957115.1:n.1539C>G
NM_006019.4:c.1401C>G MANE Select	NP_006010.2:p.Arg467=
NM_001351059.2:c.507C>G	NP_001337988.1:p.Arg169=
NM_006053.4:c.753C>G	NP_006044.1:p.Arg251=