Canonical Allele Identifier: CA381584656

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047962-G-T
• MyVariant Identifiers: chr11:g.67815429G>T (hg19) ; chr11:g.68047962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047962G>T , CM000673.2:g.68047962G>T	GRCh38
NC_000011.9:g.67815429G>T , CM000673.1:g.67815429G>T	GRCh37
NC_000011.8:g.67572005G>T	NCBI36
NG_007878.1:g.13947G>T , LRG_115:g.13947G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.169G>T
ENST00000698254.1:c.1073G>T	ENSP00000513629.1:p.Gly358Val
ENST00000698255.1:c.1493G>T	ENSP00000513630.1:p.Gly498Val
ENST00000698256.1:c.1010G>T
ENST00000698257.1:n.962G>T
ENST00000698258.1:n.679G>T
ENST00000698259.1:n.445G>T
ENST00000265686.8:c.1544G>T MANE Select	ENSP00000265686.3:p.Gly515Val
ENST00000265686.7:c.1544G>T	ENSP00000265686.3:p.Gly515Val
ENST00000525516.1:n.338G>T
ENST00000525724.5:n.856G>T
ENST00000528981.5:c.696G>T
ENST00000532635.5:c.896G>T	ENSP00000434407.1:p.Gly299Val
ENST00000533005.5:n.657G>T
NM_006019.3:c.1544G>T	NP_006010.2:p.Gly515Val
NM_006053.3:c.896G>T	NP_006044.1:p.Gly299Val
XM_005273709.2:c.1544G>T	XP_005273766.1:p.Gly515Val
XM_011544726.1:c.1544G>T	XP_011543028.1:p.Gly515Val
XM_011544727.1:c.1544G>T	XP_011543029.1:p.Gly515Val
XM_011544728.1:c.1544G>T	XP_011543030.1:p.Gly515Val
XR_949754.1:n.1548G>T
NM_001351059.1:c.650G>T	NP_001337988.1:p.Gly217Val
XM_024448320.1:c.1637G>T	XP_024304088.1:p.Gly546Val
XM_024448321.1:c.1637G>T	XP_024304089.1:p.Gly546Val
XM_024448322.1:c.1637G>T	XP_024304090.1:p.Gly546Val
XM_024448323.1:c.1637G>T	XP_024304091.1:p.Gly546Val
XM_024448324.1:c.1637G>T	XP_024304092.1:p.Gly546Val
XR_001747721.2:n.1668G>T
XR_001747722.1:n.1681G>T
XR_001747723.2:n.1681G>T
XR_002957115.1:n.1759G>T
NM_006019.4:c.1544G>T MANE Select	NP_006010.2:p.Gly515Val
NM_001351059.2:c.650G>T	NP_001337988.1:p.Gly217Val
NM_006053.4:c.896G>T	NP_006044.1:p.Gly299Val