Canonical Allele Identifier: CA381585272

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816413T>G (hg19) ; chr11:g.68048946T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048946T>G , CM000673.2:g.68048946T>G	GRCh38
NC_000011.9:g.67816413T>G , CM000673.1:g.67816413T>G	GRCh37
NC_000011.8:g.67572989T>G	NCBI36
NG_007878.1:g.14931T>G , LRG_115:g.14931T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.247T>G
ENST00000698254.1:c.1151T>G	ENSP00000513629.1:p.Leu384Arg
ENST00000698255.1:c.1571T>G	ENSP00000513630.1:p.Leu524Arg
ENST00000698256.1:c.1088T>G
ENST00000698257.1:n.1040T>G
ENST00000698258.1:n.757T>G
ENST00000698259.1:n.523T>G
ENST00000265686.8:c.1622T>G MANE Select	ENSP00000265686.3:p.Leu541Arg
ENST00000265686.7:c.1622T>G	ENSP00000265686.3:p.Leu541Arg
ENST00000525724.5:n.934T>G
ENST00000532635.5:c.974T>G	ENSP00000434407.1:p.Leu325Arg
ENST00000533005.5:n.735T>G
NM_006019.3:c.1622T>G	NP_006010.2:p.Leu541Arg
NM_006053.3:c.974T>G	NP_006044.1:p.Leu325Arg
XM_005273709.2:c.1622T>G	XP_005273766.1:p.Leu541Arg
XM_011544726.1:c.1622T>G	XP_011543028.1:p.Leu541Arg
XM_011544727.1:c.1622T>G	XP_011543029.1:p.Leu541Arg
XM_011544728.1:c.1622T>G	XP_011543030.1:p.Leu541Arg
XR_949754.1:n.1626T>G
NM_001351059.1:c.728T>G	NP_001337988.1:p.Leu243Arg
XM_024448320.1:c.1715T>G	XP_024304088.1:p.Leu572Arg
XM_024448321.1:c.1715T>G	XP_024304089.1:p.Leu572Arg
XM_024448322.1:c.1715T>G	XP_024304090.1:p.Leu572Arg
XM_024448323.1:c.1715T>G	XP_024304091.1:p.Leu572Arg
XM_024448324.1:c.1715T>G	XP_024304092.1:p.Leu572Arg
XR_001747721.2:n.1746T>G
XR_001747722.1:n.1759T>G
XR_001747723.2:n.1759T>G
XR_002957115.1:n.1837T>G
NM_006019.4:c.1622T>G MANE Select	NP_006010.2:p.Leu541Arg
NM_001351059.2:c.728T>G	NP_001337988.1:p.Leu243Arg
NM_006053.4:c.974T>G	NP_006044.1:p.Leu325Arg