Canonical Allele Identifier: CA475450221

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816408C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048941C>G , CM000673.2:g.68048941C>G	GRCh38
NC_000011.9:g.67816408C>G , CM000673.1:g.67816408C>G	GRCh37
NC_000011.8:g.67572984C>G	NCBI36
NG_007878.1:g.14926C>G , LRG_115:g.14926C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.242C>G
ENST00000698254.1:c.1146C>G	ENSP00000513629.1:p.Val382=
ENST00000698255.1:c.1566C>G	ENSP00000513630.1:p.Val522=
ENST00000698256.1:c.1083C>G
ENST00000698257.1:n.1035C>G
ENST00000698258.1:n.752C>G
ENST00000698259.1:n.518C>G
ENST00000265686.8:c.1617C>G MANE Select	ENSP00000265686.3:p.Val539=
ENST00000265686.7:c.1617C>G	ENSP00000265686.3:p.Val539=
ENST00000525724.5:n.929C>G
ENST00000532635.5:c.969C>G	ENSP00000434407.1:p.Val323=
ENST00000533005.5:n.730C>G
NM_006019.3:c.1617C>G	NP_006010.2:p.Val539=
NM_006053.3:c.969C>G	NP_006044.1:p.Val323=
XM_005273709.2:c.1617C>G	XP_005273766.1:p.Val539=
XM_011544726.1:c.1617C>G	XP_011543028.1:p.Val539=
XM_011544727.1:c.1617C>G	XP_011543029.1:p.Val539=
XM_011544728.1:c.1617C>G	XP_011543030.1:p.Val539=
XR_949754.1:n.1621C>G
NM_001351059.1:c.723C>G	NP_001337988.1:p.Val241=
XM_024448320.1:c.1710C>G	XP_024304088.1:p.Val570=
XM_024448321.1:c.1710C>G	XP_024304089.1:p.Val570=
XM_024448322.1:c.1710C>G	XP_024304090.1:p.Val570=
XM_024448323.1:c.1710C>G	XP_024304091.1:p.Val570=
XM_024448324.1:c.1710C>G	XP_024304092.1:p.Val570=
XR_001747721.2:n.1741C>G
XR_001747722.1:n.1754C>G
XR_001747723.2:n.1754C>G
XR_002957115.1:n.1832C>G
NM_006019.4:c.1617C>G MANE Select	NP_006010.2:p.Val539=
NM_001351059.2:c.723C>G	NP_001337988.1:p.Val241=
NM_006053.4:c.969C>G	NP_006044.1:p.Val323=