Canonical Allele Identifier: CA475514064

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815197G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047730G>A , CM000673.2:g.68047730G>A	GRCh38
NC_000011.9:g.67815197G>A , CM000673.1:g.67815197G>A	GRCh37
NC_000011.8:g.67571773G>A	NCBI36
NG_007878.1:g.13715G>A , LRG_115:g.13715G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.14G>A
ENST00000698254.1:c.918G>A	ENSP00000513629.1:p.Glu306=
ENST00000698255.1:c.1338G>A	ENSP00000513630.1:p.Glu446=
ENST00000698256.1:c.855G>A
ENST00000698257.1:n.807G>A
ENST00000698258.1:n.447G>A
ENST00000698259.1:n.213G>A
ENST00000265686.8:c.1389G>A MANE Select	ENSP00000265686.3:p.Glu463=
ENST00000265686.7:c.1389G>A	ENSP00000265686.3:p.Glu463=
ENST00000525516.1:n.183G>A
ENST00000525724.5:n.701G>A
ENST00000528981.5:c.541G>A
ENST00000529364.1:c.800G>A
ENST00000532635.5:c.741G>A	ENSP00000434407.1:p.Glu247=
ENST00000533005.5:n.425G>A
NM_006019.3:c.1389G>A	NP_006010.2:p.Glu463=
NM_006053.3:c.741G>A	NP_006044.1:p.Glu247=
XM_005273709.2:c.1389G>A	XP_005273766.1:p.Glu463=
XM_011544726.1:c.1389G>A	XP_011543028.1:p.Glu463=
XM_011544727.1:c.1389G>A	XP_011543029.1:p.Glu463=
XM_011544728.1:c.1389G>A	XP_011543030.1:p.Glu463=
XM_011544729.1:c.1405G>A	XP_011543031.1:p.Val469Met
XR_949754.1:n.1393G>A
NM_001351059.1:c.495G>A	NP_001337988.1:p.Glu165=
XM_024448320.1:c.1405G>A	XP_024304088.1:p.Val469Met
XM_024448321.1:c.1405G>A	XP_024304089.1:p.Val469Met
XM_024448322.1:c.1405G>A	XP_024304090.1:p.Val469Met
XM_024448323.1:c.1405G>A	XP_024304091.1:p.Val469Met
XM_024448324.1:c.1405G>A	XP_024304092.1:p.Val469Met
XR_001747721.2:n.1513G>A
XR_001747722.1:n.1526G>A
XR_001747723.2:n.1526G>A
XR_002957115.1:n.1527G>A
NM_006019.4:c.1389G>A MANE Select	NP_006010.2:p.Glu463=
NM_001351059.2:c.495G>A	NP_001337988.1:p.Glu165=
NM_006053.4:c.741G>A	NP_006044.1:p.Glu247=