Canonical Allele Identifier: CA475513888

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 2709275
• ClinVar RCV Id: RCV003547924
• gnomAD v4: 11-68047682-C-G
• MyVariant Identifiers: chr11:g.67815149C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047682C>G , CM000673.2:g.68047682C>G	GRCh38
NC_000011.9:g.67815149C>G , CM000673.1:g.67815149C>G	GRCh37
NC_000011.8:g.67571725C>G	NCBI36
NG_007878.1:g.13667C>G , LRG_115:g.13667C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.870C>G	ENSP00000513629.1:p.Leu290=
ENST00000698255.1:c.1290C>G	ENSP00000513630.1:p.Leu430=
ENST00000698256.1:c.807C>G
ENST00000698257.1:n.759C>G
ENST00000698258.1:n.399C>G
ENST00000698259.1:n.165C>G
ENST00000265686.8:c.1341C>G MANE Select	ENSP00000265686.3:p.Leu447=
ENST00000265686.7:c.1341C>G	ENSP00000265686.3:p.Leu447=
ENST00000525516.1:n.135C>G
ENST00000525724.5:n.653C>G
ENST00000528981.5:c.493C>G
ENST00000529364.1:c.752C>G
ENST00000532635.5:c.693C>G	ENSP00000434407.1:p.Leu231=
ENST00000533005.5:n.377C>G
NM_006019.3:c.1341C>G	NP_006010.2:p.Leu447=
NM_006053.3:c.693C>G	NP_006044.1:p.Leu231=
XM_005273709.2:c.1341C>G	XP_005273766.1:p.Leu447=
XM_011544726.1:c.1341C>G	XP_011543028.1:p.Leu447=
XM_011544727.1:c.1341C>G	XP_011543029.1:p.Leu447=
XM_011544728.1:c.1341C>G	XP_011543030.1:p.Leu447=
XM_011544729.1:c.1357C>G	XP_011543031.1:p.Pro453Ala
XR_949754.1:n.1345C>G
NM_001351059.1:c.447C>G	NP_001337988.1:p.Leu149=
XM_024448320.1:c.1357C>G	XP_024304088.1:p.Pro453Ala
XM_024448321.1:c.1357C>G	XP_024304089.1:p.Pro453Ala
XM_024448322.1:c.1357C>G	XP_024304090.1:p.Pro453Ala
XM_024448323.1:c.1357C>G	XP_024304091.1:p.Pro453Ala
XM_024448324.1:c.1357C>G	XP_024304092.1:p.Pro453Ala
XR_001747721.2:n.1465C>G
XR_001747722.1:n.1478C>G
XR_001747723.2:n.1478C>G
XR_002957115.1:n.1479C>G
NM_006019.4:c.1341C>G MANE Select	NP_006010.2:p.Leu447=
NM_001351059.2:c.447C>G	NP_001337988.1:p.Leu149=
NM_006053.4:c.693C>G	NP_006044.1:p.Leu231=