Canonical Allele Identifier: CA381584590

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1855591963
• gnomAD v4: 11-68047935-G-T
• MyVariant Identifiers: chr11:g.67815402G>T (hg19) ; chr11:g.68047935G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047935G>T , CM000673.2:g.68047935G>T	GRCh38
NC_000011.9:g.67815402G>T , CM000673.1:g.67815402G>T	GRCh37
NC_000011.8:g.67571978G>T	NCBI36
NG_007878.1:g.13920G>T , LRG_115:g.13920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.142G>T
ENST00000698254.1:c.1046G>T	ENSP00000513629.1:p.Gly349Val
ENST00000698255.1:c.1466G>T	ENSP00000513630.1:p.Gly489Val
ENST00000698256.1:c.983G>T
ENST00000698257.1:n.935G>T
ENST00000698258.1:n.652G>T
ENST00000698259.1:n.418G>T
ENST00000265686.8:c.1517G>T MANE Select	ENSP00000265686.3:p.Gly506Val
ENST00000265686.7:c.1517G>T	ENSP00000265686.3:p.Gly506Val
ENST00000525516.1:n.311G>T
ENST00000525724.5:n.829G>T
ENST00000528981.5:c.669G>T
ENST00000532635.5:c.869G>T	ENSP00000434407.1:p.Gly290Val
ENST00000533005.5:n.630G>T
NM_006019.3:c.1517G>T	NP_006010.2:p.Gly506Val
NM_006053.3:c.869G>T	NP_006044.1:p.Gly290Val
XM_005273709.2:c.1517G>T	XP_005273766.1:p.Gly506Val
XM_011544726.1:c.1517G>T	XP_011543028.1:p.Gly506Val
XM_011544727.1:c.1517G>T	XP_011543029.1:p.Gly506Val
XM_011544728.1:c.1517G>T	XP_011543030.1:p.Gly506Val
XR_949754.1:n.1521G>T
NM_001351059.1:c.623G>T	NP_001337988.1:p.Gly208Val
XM_024448320.1:c.1610G>T	XP_024304088.1:p.Gly537Val
XM_024448321.1:c.1610G>T	XP_024304089.1:p.Gly537Val
XM_024448322.1:c.1610G>T	XP_024304090.1:p.Gly537Val
XM_024448323.1:c.1610G>T	XP_024304091.1:p.Gly537Val
XM_024448324.1:c.1610G>T	XP_024304092.1:p.Gly537Val
XR_001747721.2:n.1641G>T
XR_001747722.1:n.1654G>T
XR_001747723.2:n.1654G>T
XR_002957115.1:n.1732G>T
NM_006019.4:c.1517G>T MANE Select	NP_006010.2:p.Gly506Val
NM_001351059.2:c.623G>T	NP_001337988.1:p.Gly208Val
NM_006053.4:c.869G>T	NP_006044.1:p.Gly290Val