Canonical Allele Identifier: CA475513930

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815382C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047915C>T , CM000673.2:g.68047915C>T	GRCh38
NC_000011.9:g.67815382C>T , CM000673.1:g.67815382C>T	GRCh37
NC_000011.8:g.67571958C>T	NCBI36
NG_007878.1:g.13900C>T , LRG_115:g.13900C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.122C>T
ENST00000698254.1:c.1026C>T	ENSP00000513629.1:p.Thr342=
ENST00000698255.1:c.1446C>T	ENSP00000513630.1:p.Thr482=
ENST00000698256.1:c.963C>T
ENST00000698257.1:n.915C>T
ENST00000698258.1:n.632C>T
ENST00000698259.1:n.398C>T
ENST00000265686.8:c.1497C>T MANE Select	ENSP00000265686.3:p.Thr499=
ENST00000265686.7:c.1497C>T	ENSP00000265686.3:p.Thr499=
ENST00000525516.1:n.291C>T
ENST00000525724.5:n.809C>T
ENST00000528981.5:c.649C>T
ENST00000532635.5:c.849C>T	ENSP00000434407.1:p.Thr283=
ENST00000533005.5:n.610C>T
NM_006019.3:c.1497C>T	NP_006010.2:p.Thr499=
NM_006053.3:c.849C>T	NP_006044.1:p.Thr283=
XM_005273709.2:c.1497C>T	XP_005273766.1:p.Thr499=
XM_011544726.1:c.1497C>T	XP_011543028.1:p.Thr499=
XM_011544727.1:c.1497C>T	XP_011543029.1:p.Thr499=
XM_011544728.1:c.1497C>T	XP_011543030.1:p.Thr499=
XR_949754.1:n.1501C>T
NM_001351059.1:c.603C>T	NP_001337988.1:p.Thr201=
XM_024448320.1:c.1590C>T	XP_024304088.1:p.Thr530=
XM_024448321.1:c.1590C>T	XP_024304089.1:p.Thr530=
XM_024448322.1:c.1590C>T	XP_024304090.1:p.Thr530=
XM_024448323.1:c.1590C>T	XP_024304091.1:p.Thr530=
XM_024448324.1:c.1590C>T	XP_024304092.1:p.Thr530=
XR_001747721.2:n.1621C>T
XR_001747722.1:n.1634C>T
XR_001747723.2:n.1634C>T
XR_002957115.1:n.1712C>T
NM_006019.4:c.1497C>T MANE Select	NP_006010.2:p.Thr499=
NM_001351059.2:c.603C>T	NP_001337988.1:p.Thr201=
NM_006053.4:c.849C>T	NP_006044.1:p.Thr283=