Canonical Allele Identifier: CA381583693

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1855573705
• MyVariant Identifiers: chr11:g.67815156A>G (hg19) ; chr11:g.68047689A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047689A>G , CM000673.2:g.68047689A>G	GRCh38
NC_000011.9:g.67815156A>G , CM000673.1:g.67815156A>G	GRCh37
NC_000011.8:g.67571732A>G	NCBI36
NG_007878.1:g.13674A>G , LRG_115:g.13674A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.877A>G	ENSP00000513629.1:p.Met293Val
ENST00000698255.1:c.1297A>G	ENSP00000513630.1:p.Met433Val
ENST00000698256.1:c.814A>G
ENST00000698257.1:n.766A>G
ENST00000698258.1:n.406A>G
ENST00000698259.1:n.172A>G
ENST00000265686.8:c.1348A>G MANE Select	ENSP00000265686.3:p.Met450Val
ENST00000265686.7:c.1348A>G	ENSP00000265686.3:p.Met450Val
ENST00000525516.1:n.142A>G
ENST00000525724.5:n.660A>G
ENST00000528981.5:c.500A>G
ENST00000529364.1:c.759A>G
ENST00000532635.5:c.700A>G	ENSP00000434407.1:p.Met234Val
ENST00000533005.5:n.384A>G
NM_006019.3:c.1348A>G	NP_006010.2:p.Met450Val
NM_006053.3:c.700A>G	NP_006044.1:p.Met234Val
XM_005273709.2:c.1348A>G	XP_005273766.1:p.Met450Val
XM_011544726.1:c.1348A>G	XP_011543028.1:p.Met450Val
XM_011544727.1:c.1348A>G	XP_011543029.1:p.Met450Val
XM_011544728.1:c.1348A>G	XP_011543030.1:p.Met450Val
XM_011544729.1:c.1364A>G	XP_011543031.1:p.Tyr455Cys
XR_949754.1:n.1352A>G
NM_001351059.1:c.454A>G	NP_001337988.1:p.Met152Val
XM_024448320.1:c.1364A>G	XP_024304088.1:p.Tyr455Cys
XM_024448321.1:c.1364A>G	XP_024304089.1:p.Tyr455Cys
XM_024448322.1:c.1364A>G	XP_024304090.1:p.Tyr455Cys
XM_024448323.1:c.1364A>G	XP_024304091.1:p.Tyr455Cys
XM_024448324.1:c.1364A>G	XP_024304092.1:p.Tyr455Cys
XR_001747721.2:n.1472A>G
XR_001747722.1:n.1485A>G
XR_001747723.2:n.1485A>G
XR_002957115.1:n.1486A>G
NM_006019.4:c.1348A>G MANE Select	NP_006010.2:p.Met450Val
NM_001351059.2:c.454A>G	NP_001337988.1:p.Met152Val
NM_006053.4:c.700A>G	NP_006044.1:p.Met234Val