Canonical Allele Identifier: CA381584682

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047970-C-G
• MyVariant Identifiers: chr11:g.67815437C>G (hg19) ; chr11:g.68047970C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047970C>G , CM000673.2:g.68047970C>G	GRCh38
NC_000011.9:g.67815437C>G , CM000673.1:g.67815437C>G	GRCh37
NC_000011.8:g.67572013C>G	NCBI36
NG_007878.1:g.13955C>G , LRG_115:g.13955C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.177C>G
ENST00000698254.1:c.1081C>G	ENSP00000513629.1:p.Pro361Ala
ENST00000698255.1:c.1501C>G	ENSP00000513630.1:p.Pro501Ala
ENST00000698256.1:c.1018C>G
ENST00000698257.1:n.970C>G
ENST00000698258.1:n.687C>G
ENST00000698259.1:n.453C>G
ENST00000265686.8:c.1552C>G MANE Select	ENSP00000265686.3:p.Pro518Ala
ENST00000265686.7:c.1552C>G	ENSP00000265686.3:p.Pro518Ala
ENST00000525516.1:n.346C>G
ENST00000525724.5:n.864C>G
ENST00000528981.5:c.704C>G
ENST00000532635.5:c.904C>G	ENSP00000434407.1:p.Pro302Ala
ENST00000533005.5:n.665C>G
NM_006019.3:c.1552C>G	NP_006010.2:p.Pro518Ala
NM_006053.3:c.904C>G	NP_006044.1:p.Pro302Ala
XM_005273709.2:c.1552C>G	XP_005273766.1:p.Pro518Ala
XM_011544726.1:c.1552C>G	XP_011543028.1:p.Pro518Ala
XM_011544727.1:c.1552C>G	XP_011543029.1:p.Pro518Ala
XM_011544728.1:c.1552C>G	XP_011543030.1:p.Pro518Ala
XR_949754.1:n.1556C>G
NM_001351059.1:c.658C>G	NP_001337988.1:p.Pro220Ala
XM_024448320.1:c.1645C>G	XP_024304088.1:p.Pro549Ala
XM_024448321.1:c.1645C>G	XP_024304089.1:p.Pro549Ala
XM_024448322.1:c.1645C>G	XP_024304090.1:p.Pro549Ala
XM_024448323.1:c.1645C>G	XP_024304091.1:p.Pro549Ala
XM_024448324.1:c.1645C>G	XP_024304092.1:p.Pro549Ala
XR_001747721.2:n.1676C>G
XR_001747722.1:n.1689C>G
XR_001747723.2:n.1689C>G
XR_002957115.1:n.1767C>G
NM_006019.4:c.1552C>G MANE Select	NP_006010.2:p.Pro518Ala
NM_001351059.2:c.658C>G	NP_001337988.1:p.Pro220Ala
NM_006053.4:c.904C>G	NP_006044.1:p.Pro302Ala