Canonical Allele Identifier: CA381585320

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816422T>G (hg19) ; chr11:g.68048955T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048955T>G , CM000673.2:g.68048955T>G	GRCh38
NC_000011.9:g.67816422T>G , CM000673.1:g.67816422T>G	GRCh37
NC_000011.8:g.67572998T>G	NCBI36
NG_007878.1:g.14940T>G , LRG_115:g.14940T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.256T>G
ENST00000698254.1:c.1160T>G	ENSP00000513629.1:p.Val387Gly
ENST00000698255.1:c.1580T>G	ENSP00000513630.1:p.Val527Gly
ENST00000698256.1:c.1097T>G
ENST00000698257.1:n.1049T>G
ENST00000698258.1:n.766T>G
ENST00000698259.1:n.532T>G
ENST00000265686.8:c.1631T>G MANE Select	ENSP00000265686.3:p.Val544Gly
ENST00000265686.7:c.1631T>G	ENSP00000265686.3:p.Val544Gly
ENST00000525724.5:n.943T>G
ENST00000532635.5:c.983T>G	ENSP00000434407.1:p.Val328Gly
ENST00000533005.5:n.744T>G
NM_006019.3:c.1631T>G	NP_006010.2:p.Val544Gly
NM_006053.3:c.983T>G	NP_006044.1:p.Val328Gly
XM_005273709.2:c.1631T>G	XP_005273766.1:p.Val544Gly
XM_011544726.1:c.1631T>G	XP_011543028.1:p.Val544Gly
XM_011544727.1:c.1631T>G	XP_011543029.1:p.Val544Gly
XM_011544728.1:c.1631T>G	XP_011543030.1:p.Val544Gly
XR_949754.1:n.1635T>G
NM_001351059.1:c.737T>G	NP_001337988.1:p.Val246Gly
XM_024448320.1:c.1724T>G	XP_024304088.1:p.Val575Gly
XM_024448321.1:c.1724T>G	XP_024304089.1:p.Val575Gly
XM_024448322.1:c.1724T>G	XP_024304090.1:p.Val575Gly
XM_024448323.1:c.1724T>G	XP_024304091.1:p.Val575Gly
XM_024448324.1:c.1724T>G	XP_024304092.1:p.Val575Gly
XR_001747721.2:n.1755T>G
XR_001747722.1:n.1768T>G
XR_001747723.2:n.1768T>G
XR_002957115.1:n.1846T>G
NM_006019.4:c.1631T>G MANE Select	NP_006010.2:p.Val544Gly
NM_001351059.2:c.737T>G	NP_001337988.1:p.Val246Gly
NM_006053.4:c.983T>G	NP_006044.1:p.Val328Gly