Canonical Allele Identifier: CA475513914

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815370C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047903C>T , CM000673.2:g.68047903C>T	GRCh38
NC_000011.9:g.67815370C>T , CM000673.1:g.67815370C>T	GRCh37
NC_000011.8:g.67571946C>T	NCBI36
NG_007878.1:g.13888C>T , LRG_115:g.13888C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.110C>T
ENST00000698254.1:c.1014C>T	ENSP00000513629.1:p.His338=
ENST00000698255.1:c.1434C>T	ENSP00000513630.1:p.His478=
ENST00000698256.1:c.951C>T
ENST00000698257.1:n.903C>T
ENST00000698258.1:n.620C>T
ENST00000698259.1:n.386C>T
ENST00000265686.8:c.1485C>T MANE Select	ENSP00000265686.3:p.His495=
ENST00000265686.7:c.1485C>T	ENSP00000265686.3:p.His495=
ENST00000525516.1:n.279C>T
ENST00000525724.5:n.797C>T
ENST00000528981.5:c.637C>T
ENST00000532635.5:c.837C>T	ENSP00000434407.1:p.His279=
ENST00000533005.5:n.598C>T
NM_006019.3:c.1485C>T	NP_006010.2:p.His495=
NM_006053.3:c.837C>T	NP_006044.1:p.His279=
XM_005273709.2:c.1485C>T	XP_005273766.1:p.His495=
XM_011544726.1:c.1485C>T	XP_011543028.1:p.His495=
XM_011544727.1:c.1485C>T	XP_011543029.1:p.His495=
XM_011544728.1:c.1485C>T	XP_011543030.1:p.His495=
XR_949754.1:n.1489C>T
NM_001351059.1:c.591C>T	NP_001337988.1:p.His197=
XM_024448320.1:c.1578C>T	XP_024304088.1:p.His526=
XM_024448321.1:c.1578C>T	XP_024304089.1:p.His526=
XM_024448322.1:c.1578C>T	XP_024304090.1:p.His526=
XM_024448323.1:c.1578C>T	XP_024304091.1:p.His526=
XM_024448324.1:c.1578C>T	XP_024304092.1:p.His526=
XR_001747721.2:n.1609C>T
XR_001747722.1:n.1622C>T
XR_001747723.2:n.1622C>T
XR_002957115.1:n.1700C>T
NM_006019.4:c.1485C>T MANE Select	NP_006010.2:p.His495=
NM_001351059.2:c.591C>T	NP_001337988.1:p.His197=
NM_006053.4:c.837C>T	NP_006044.1:p.His279=