Canonical Allele Identifier: CA475514021

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 1551113
• ClinVar RCV Id: RCV002192201
• dbSNP Id: rs1352497123
• gnomAD v2: 11-67815418-C-G
• gnomAD v4: 11-68047951-C-G
• MyVariant Identifiers: chr11:g.67815418C>G (hg19) ; chr11:g.68047951C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047951C>G , CM000673.2:g.68047951C>G	GRCh38
NC_000011.9:g.67815418C>G , CM000673.1:g.67815418C>G	GRCh37
NC_000011.8:g.67571994C>G	NCBI36
NG_007878.1:g.13936C>G , LRG_115:g.13936C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.158C>G
ENST00000698254.1:c.1062C>G	ENSP00000513629.1:p.Pro354=
ENST00000698255.1:c.1482C>G	ENSP00000513630.1:p.Pro494=
ENST00000698256.1:c.999C>G
ENST00000698257.1:n.951C>G
ENST00000698258.1:n.668C>G
ENST00000698259.1:n.434C>G
ENST00000265686.8:c.1533C>G MANE Select	ENSP00000265686.3:p.Pro511=
ENST00000265686.7:c.1533C>G	ENSP00000265686.3:p.Pro511=
ENST00000525516.1:n.327C>G
ENST00000525724.5:n.845C>G
ENST00000528981.5:c.685C>G
ENST00000532635.5:c.885C>G	ENSP00000434407.1:p.Pro295=
ENST00000533005.5:n.646C>G
NM_006019.3:c.1533C>G	NP_006010.2:p.Pro511=
NM_006053.3:c.885C>G	NP_006044.1:p.Pro295=
XM_005273709.2:c.1533C>G	XP_005273766.1:p.Pro511=
XM_011544726.1:c.1533C>G	XP_011543028.1:p.Pro511=
XM_011544727.1:c.1533C>G	XP_011543029.1:p.Pro511=
XM_011544728.1:c.1533C>G	XP_011543030.1:p.Pro511=
XR_949754.1:n.1537C>G
NM_001351059.1:c.639C>G	NP_001337988.1:p.Pro213=
XM_024448320.1:c.1626C>G	XP_024304088.1:p.Pro542=
XM_024448321.1:c.1626C>G	XP_024304089.1:p.Pro542=
XM_024448322.1:c.1626C>G	XP_024304090.1:p.Pro542=
XM_024448323.1:c.1626C>G	XP_024304091.1:p.Pro542=
XM_024448324.1:c.1626C>G	XP_024304092.1:p.Pro542=
XR_001747721.2:n.1657C>G
XR_001747722.1:n.1670C>G
XR_001747723.2:n.1670C>G
XR_002957115.1:n.1748C>G
NM_006019.4:c.1533C>G MANE Select	NP_006010.2:p.Pro511=
NM_001351059.2:c.639C>G	NP_001337988.1:p.Pro213=
NM_006053.4:c.885C>G	NP_006044.1:p.Pro295=