Canonical Allele Identifier: CA381584248

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815253C>G (hg19) ; chr11:g.68047786C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047786C>G , CM000673.2:g.68047786C>G	GRCh38
NC_000011.9:g.67815253C>G , CM000673.1:g.67815253C>G	GRCh37
NC_000011.8:g.67571829C>G	NCBI36
NG_007878.1:g.13771C>G , LRG_115:g.13771C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.70C>G
ENST00000698254.1:c.974C>G	ENSP00000513629.1:p.Ala325Gly
ENST00000698255.1:c.1394C>G	ENSP00000513630.1:p.Ala465Gly
ENST00000698256.1:c.911C>G
ENST00000698257.1:n.863C>G
ENST00000698258.1:n.503C>G
ENST00000698259.1:n.269C>G
ENST00000265686.8:c.1445C>G MANE Select	ENSP00000265686.3:p.Ala482Gly
ENST00000265686.7:c.1445C>G	ENSP00000265686.3:p.Ala482Gly
ENST00000525516.1:n.239C>G
ENST00000525724.5:n.757C>G
ENST00000528981.5:c.597C>G
ENST00000529364.1:c.856C>G
ENST00000532635.5:c.797C>G	ENSP00000434407.1:p.Ala266Gly
ENST00000533005.5:n.481C>G
NM_006019.3:c.1445C>G	NP_006010.2:p.Ala482Gly
NM_006053.3:c.797C>G	NP_006044.1:p.Ala266Gly
XM_005273709.2:c.1445C>G	XP_005273766.1:p.Ala482Gly
XM_011544726.1:c.1445C>G	XP_011543028.1:p.Ala482Gly
XM_011544727.1:c.1445C>G	XP_011543029.1:p.Ala482Gly
XM_011544728.1:c.1445C>G	XP_011543030.1:p.Ala482Gly
XM_011544729.1:c.1461C>G	XP_011543031.1:p.Gly487=
XR_949754.1:n.1449C>G
NM_001351059.1:c.551C>G	NP_001337988.1:p.Ala184Gly
XM_024448320.1:c.1461C>G	XP_024304088.1:p.Gly487=
XM_024448321.1:c.1461C>G	XP_024304089.1:p.Gly487=
XM_024448322.1:c.1461C>G	XP_024304090.1:p.Gly487=
XM_024448323.1:c.1461C>G	XP_024304091.1:p.Gly487=
XM_024448324.1:c.1461C>G	XP_024304092.1:p.Gly487=
XR_001747721.2:n.1569C>G
XR_001747722.1:n.1582C>G
XR_001747723.2:n.1582C>G
XR_002957115.1:n.1583C>G
NM_006019.4:c.1445C>G MANE Select	NP_006010.2:p.Ala482Gly
NM_001351059.2:c.551C>G	NP_001337988.1:p.Ala184Gly
NM_006053.4:c.797C>G	NP_006044.1:p.Ala266Gly