Canonical Allele Identifier: CA475514077

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815215C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047748C>G , CM000673.2:g.68047748C>G	GRCh38
NC_000011.9:g.67815215C>G , CM000673.1:g.67815215C>G	GRCh37
NC_000011.8:g.67571791C>G	NCBI36
NG_007878.1:g.13733C>G , LRG_115:g.13733C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.32C>G
ENST00000698254.1:c.936C>G	ENSP00000513629.1:p.Thr312=
ENST00000698255.1:c.1356C>G	ENSP00000513630.1:p.Thr452=
ENST00000698256.1:c.873C>G
ENST00000698257.1:n.825C>G
ENST00000698258.1:n.465C>G
ENST00000698259.1:n.231C>G
ENST00000265686.8:c.1407C>G MANE Select	ENSP00000265686.3:p.Thr469=
ENST00000265686.7:c.1407C>G	ENSP00000265686.3:p.Thr469=
ENST00000525516.1:n.201C>G
ENST00000525724.5:n.719C>G
ENST00000528981.5:c.559C>G
ENST00000529364.1:c.818C>G
ENST00000532635.5:c.759C>G	ENSP00000434407.1:p.Thr253=
ENST00000533005.5:n.443C>G
NM_006019.3:c.1407C>G	NP_006010.2:p.Thr469=
NM_006053.3:c.759C>G	NP_006044.1:p.Thr253=
XM_005273709.2:c.1407C>G	XP_005273766.1:p.Thr469=
XM_011544726.1:c.1407C>G	XP_011543028.1:p.Thr469=
XM_011544727.1:c.1407C>G	XP_011543029.1:p.Thr469=
XM_011544728.1:c.1407C>G	XP_011543030.1:p.Thr469=
XM_011544729.1:c.1423C>G	XP_011543031.1:p.Gln475Glu
XR_949754.1:n.1411C>G
NM_001351059.1:c.513C>G	NP_001337988.1:p.Thr171=
XM_024448320.1:c.1423C>G	XP_024304088.1:p.Gln475Glu
XM_024448321.1:c.1423C>G	XP_024304089.1:p.Gln475Glu
XM_024448322.1:c.1423C>G	XP_024304090.1:p.Gln475Glu
XM_024448323.1:c.1423C>G	XP_024304091.1:p.Gln475Glu
XM_024448324.1:c.1423C>G	XP_024304092.1:p.Gln475Glu
XR_001747721.2:n.1531C>G
XR_001747722.1:n.1544C>G
XR_001747723.2:n.1544C>G
XR_002957115.1:n.1545C>G
NM_006019.4:c.1407C>G MANE Select	NP_006010.2:p.Thr469=
NM_001351059.2:c.513C>G	NP_001337988.1:p.Thr171=
NM_006053.4:c.759C>G	NP_006044.1:p.Thr253=