Canonical Allele Identifier: CA475450174

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816390C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048923C>T , CM000673.2:g.68048923C>T	GRCh38
NC_000011.9:g.67816390C>T , CM000673.1:g.67816390C>T	GRCh37
NC_000011.8:g.67572966C>T	NCBI36
NG_007878.1:g.14908C>T , LRG_115:g.14908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.224C>T
ENST00000698254.1:c.1128C>T	ENSP00000513629.1:p.Phe376=
ENST00000698255.1:c.1548C>T	ENSP00000513630.1:p.Phe516=
ENST00000698256.1:c.1065C>T
ENST00000698257.1:n.1017C>T
ENST00000698258.1:n.734C>T
ENST00000698259.1:n.500C>T
ENST00000265686.8:c.1599C>T MANE Select	ENSP00000265686.3:p.Phe533=
ENST00000265686.7:c.1599C>T	ENSP00000265686.3:p.Phe533=
ENST00000525724.5:n.911C>T
ENST00000528981.5:c.751C>T
ENST00000532635.5:c.951C>T	ENSP00000434407.1:p.Phe317=
ENST00000533005.5:n.712C>T
NM_006019.3:c.1599C>T	NP_006010.2:p.Phe533=
NM_006053.3:c.951C>T	NP_006044.1:p.Phe317=
XM_005273709.2:c.1599C>T	XP_005273766.1:p.Phe533=
XM_011544726.1:c.1599C>T	XP_011543028.1:p.Phe533=
XM_011544727.1:c.1599C>T	XP_011543029.1:p.Phe533=
XM_011544728.1:c.1599C>T	XP_011543030.1:p.Phe533=
XR_949754.1:n.1603C>T
NM_001351059.1:c.705C>T	NP_001337988.1:p.Phe235=
XM_024448320.1:c.1692C>T	XP_024304088.1:p.Phe564=
XM_024448321.1:c.1692C>T	XP_024304089.1:p.Phe564=
XM_024448322.1:c.1692C>T	XP_024304090.1:p.Phe564=
XM_024448323.1:c.1692C>T	XP_024304091.1:p.Phe564=
XM_024448324.1:c.1692C>T	XP_024304092.1:p.Phe564=
XR_001747721.2:n.1723C>T
XR_001747722.1:n.1736C>T
XR_001747723.2:n.1736C>T
XR_002957115.1:n.1814C>T
NM_006019.4:c.1599C>T MANE Select	NP_006010.2:p.Phe533=
NM_001351059.2:c.705C>T	NP_001337988.1:p.Phe235=
NM_006053.4:c.951C>T	NP_006044.1:p.Phe317=