Canonical Allele Identifier: CA381584123

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815231G>T (hg19) ; chr11:g.68047764G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047764G>T , CM000673.2:g.68047764G>T	GRCh38
NC_000011.9:g.67815231G>T , CM000673.1:g.67815231G>T	GRCh37
NC_000011.8:g.67571807G>T	NCBI36
NG_007878.1:g.13749G>T , LRG_115:g.13749G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.48G>T
ENST00000698254.1:c.952G>T	ENSP00000513629.1:p.Gly318Cys
ENST00000698255.1:c.1372G>T	ENSP00000513630.1:p.Gly458Cys
ENST00000698256.1:c.889G>T
ENST00000698257.1:n.841G>T
ENST00000698258.1:n.481G>T
ENST00000698259.1:n.247G>T
ENST00000265686.8:c.1423G>T MANE Select	ENSP00000265686.3:p.Gly475Cys
ENST00000265686.7:c.1423G>T	ENSP00000265686.3:p.Gly475Cys
ENST00000525516.1:n.217G>T
ENST00000525724.5:n.735G>T
ENST00000528981.5:c.575G>T
ENST00000529364.1:c.834G>T
ENST00000532635.5:c.775G>T	ENSP00000434407.1:p.Gly259Cys
ENST00000533005.5:n.459G>T
NM_006019.3:c.1423G>T	NP_006010.2:p.Gly475Cys
NM_006053.3:c.775G>T	NP_006044.1:p.Gly259Cys
XM_005273709.2:c.1423G>T	XP_005273766.1:p.Gly475Cys
XM_011544726.1:c.1423G>T	XP_011543028.1:p.Gly475Cys
XM_011544727.1:c.1423G>T	XP_011543029.1:p.Gly475Cys
XM_011544728.1:c.1423G>T	XP_011543030.1:p.Gly475Cys
XM_011544729.1:c.1439G>T	XP_011543031.1:p.Gly480Val
XR_949754.1:n.1427G>T
NM_001351059.1:c.529G>T	NP_001337988.1:p.Gly177Cys
XM_024448320.1:c.1439G>T	XP_024304088.1:p.Gly480Val
XM_024448321.1:c.1439G>T	XP_024304089.1:p.Gly480Val
XM_024448322.1:c.1439G>T	XP_024304090.1:p.Gly480Val
XM_024448323.1:c.1439G>T	XP_024304091.1:p.Gly480Val
XM_024448324.1:c.1439G>T	XP_024304092.1:p.Gly480Val
XR_001747721.2:n.1547G>T
XR_001747722.1:n.1560G>T
XR_001747723.2:n.1560G>T
XR_002957115.1:n.1561G>T
NM_006019.4:c.1423G>T MANE Select	NP_006010.2:p.Gly475Cys
NM_001351059.2:c.529G>T	NP_001337988.1:p.Gly177Cys
NM_006053.4:c.775G>T	NP_006044.1:p.Gly259Cys