Canonical Allele Identifier: CA381584614

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815414G>T (hg19) ; chr11:g.68047947G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047947G>T , CM000673.2:g.68047947G>T	GRCh38
NC_000011.9:g.67815414G>T , CM000673.1:g.67815414G>T	GRCh37
NC_000011.8:g.67571990G>T	NCBI36
NG_007878.1:g.13932G>T , LRG_115:g.13932G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.154G>T
ENST00000698254.1:c.1058G>T	ENSP00000513629.1:p.Gly353Val
ENST00000698255.1:c.1478G>T	ENSP00000513630.1:p.Gly493Val
ENST00000698256.1:c.995G>T
ENST00000698257.1:n.947G>T
ENST00000698258.1:n.664G>T
ENST00000698259.1:n.430G>T
ENST00000265686.8:c.1529G>T MANE Select	ENSP00000265686.3:p.Gly510Val
ENST00000265686.7:c.1529G>T	ENSP00000265686.3:p.Gly510Val
ENST00000525516.1:n.323G>T
ENST00000525724.5:n.841G>T
ENST00000528981.5:c.681G>T
ENST00000532635.5:c.881G>T	ENSP00000434407.1:p.Gly294Val
ENST00000533005.5:n.642G>T
NM_006019.3:c.1529G>T	NP_006010.2:p.Gly510Val
NM_006053.3:c.881G>T	NP_006044.1:p.Gly294Val
XM_005273709.2:c.1529G>T	XP_005273766.1:p.Gly510Val
XM_011544726.1:c.1529G>T	XP_011543028.1:p.Gly510Val
XM_011544727.1:c.1529G>T	XP_011543029.1:p.Gly510Val
XM_011544728.1:c.1529G>T	XP_011543030.1:p.Gly510Val
XR_949754.1:n.1533G>T
NM_001351059.1:c.635G>T	NP_001337988.1:p.Gly212Val
XM_024448320.1:c.1622G>T	XP_024304088.1:p.Gly541Val
XM_024448321.1:c.1622G>T	XP_024304089.1:p.Gly541Val
XM_024448322.1:c.1622G>T	XP_024304090.1:p.Gly541Val
XM_024448323.1:c.1622G>T	XP_024304091.1:p.Gly541Val
XM_024448324.1:c.1622G>T	XP_024304092.1:p.Gly541Val
XR_001747721.2:n.1653G>T
XR_001747722.1:n.1666G>T
XR_001747723.2:n.1666G>T
XR_002957115.1:n.1744G>T
NM_006019.4:c.1529G>T MANE Select	NP_006010.2:p.Gly510Val
NM_001351059.2:c.635G>T	NP_001337988.1:p.Gly212Val
NM_006053.4:c.881G>T	NP_006044.1:p.Gly294Val