Canonical Allele Identifier: CA475514049

Gene: TCIRG1

Linked Data

• dbSNP Id: rs2134456293
• gnomAD v3: 11-68047963-C-A
• gnomAD v4: 11-68047963-C-A
• MyVariant Identifiers: chr11:g.67815430C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047963C>A , CM000673.2:g.68047963C>A	GRCh38
NC_000011.9:g.67815430C>A , CM000673.1:g.67815430C>A	GRCh37
NC_000011.8:g.67572006C>A	NCBI36
NG_007878.1:g.13948C>A , LRG_115:g.13948C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.170C>A
ENST00000698254.1:c.1074C>A	ENSP00000513629.1:p.Gly358=
ENST00000698255.1:c.1494C>A	ENSP00000513630.1:p.Gly498=
ENST00000698256.1:c.1011C>A
ENST00000698257.1:n.963C>A
ENST00000698258.1:n.680C>A
ENST00000698259.1:n.446C>A
ENST00000265686.8:c.1545C>A MANE Select	ENSP00000265686.3:p.Gly515=
ENST00000265686.7:c.1545C>A	ENSP00000265686.3:p.Gly515=
ENST00000525516.1:n.339C>A
ENST00000525724.5:n.857C>A
ENST00000528981.5:c.697C>A
ENST00000532635.5:c.897C>A	ENSP00000434407.1:p.Gly299=
ENST00000533005.5:n.658C>A
NM_006019.3:c.1545C>A	NP_006010.2:p.Gly515=
NM_006053.3:c.897C>A	NP_006044.1:p.Gly299=
XM_005273709.2:c.1545C>A	XP_005273766.1:p.Gly515=
XM_011544726.1:c.1545C>A	XP_011543028.1:p.Gly515=
XM_011544727.1:c.1545C>A	XP_011543029.1:p.Gly515=
XM_011544728.1:c.1545C>A	XP_011543030.1:p.Gly515=
XR_949754.1:n.1549C>A
NM_001351059.1:c.651C>A	NP_001337988.1:p.Gly217=
XM_024448320.1:c.1638C>A	XP_024304088.1:p.Gly546=
XM_024448321.1:c.1638C>A	XP_024304089.1:p.Gly546=
XM_024448322.1:c.1638C>A	XP_024304090.1:p.Gly546=
XM_024448323.1:c.1638C>A	XP_024304091.1:p.Gly546=
XM_024448324.1:c.1638C>A	XP_024304092.1:p.Gly546=
XR_001747721.2:n.1669C>A
XR_001747722.1:n.1682C>A
XR_001747723.2:n.1682C>A
XR_002957115.1:n.1760C>A
NM_006019.4:c.1545C>A MANE Select	NP_006010.2:p.Gly515=
NM_001351059.2:c.651C>A	NP_001337988.1:p.Gly217=
NM_006053.4:c.897C>A	NP_006044.1:p.Gly299=