Canonical Allele Identifier: CA381584684

Gene: TCIRG1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.177C>T
ENST00000698254.1:c.1081C>T	ENSP00000513629.1:p.Pro361Ser
ENST00000698255.1:c.1501C>T	ENSP00000513630.1:p.Pro501Ser
ENST00000698256.1:c.1018C>T
ENST00000698257.1:n.970C>T
ENST00000698258.1:n.687C>T
ENST00000698259.1:n.453C>T
ENST00000265686.8:c.1552C>T MANE Select	ENSP00000265686.3:p.Pro518Ser
ENST00000265686.7:c.1552C>T	ENSP00000265686.3:p.Pro518Ser
ENST00000525516.1:n.346C>T
ENST00000525724.5:n.864C>T
ENST00000528981.5:c.704C>T
ENST00000532635.5:c.904C>T	ENSP00000434407.1:p.Pro302Ser
ENST00000533005.5:n.665C>T
NM_006019.3:c.1552C>T	NP_006010.2:p.Pro518Ser
NM_006053.3:c.904C>T	NP_006044.1:p.Pro302Ser
XM_005273709.2:c.1552C>T	XP_005273766.1:p.Pro518Ser
XM_011544726.1:c.1552C>T	XP_011543028.1:p.Pro518Ser
XM_011544727.1:c.1552C>T	XP_011543029.1:p.Pro518Ser
XM_011544728.1:c.1552C>T	XP_011543030.1:p.Pro518Ser
XR_949754.1:n.1556C>T
NM_001351059.1:c.658C>T	NP_001337988.1:p.Pro220Ser
XM_024448320.1:c.1645C>T	XP_024304088.1:p.Pro549Ser
XM_024448321.1:c.1645C>T	XP_024304089.1:p.Pro549Ser
XM_024448322.1:c.1645C>T	XP_024304090.1:p.Pro549Ser
XM_024448323.1:c.1645C>T	XP_024304091.1:p.Pro549Ser
XM_024448324.1:c.1645C>T	XP_024304092.1:p.Pro549Ser
XR_001747721.2:n.1676C>T
XR_001747722.1:n.1689C>T
XR_001747723.2:n.1689C>T
XR_002957115.1:n.1767C>T
NM_006019.4:c.1552C>T MANE Select	NP_006010.2:p.Pro518Ser
NM_001351059.2:c.658C>T	NP_001337988.1:p.Pro220Ser
NM_006053.4:c.904C>T	NP_006044.1:p.Pro302Ser