Canonical Allele Identifier: CA224209455

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 1537131
• ClinVar RCV Id: RCV002157073
• dbSNP Id: rs376351835
• MyVariant Identifiers: chr11:g.67816378C>T (hg19) ; chr11:g.68048911C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048911C>T , CM000673.2:g.68048911C>T	GRCh38
NC_000011.9:g.67816378C>T , CM000673.1:g.67816378C>T	GRCh37
NC_000011.8:g.67572954C>T	NCBI36
NG_007878.1:g.14896C>T , LRG_115:g.14896C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.212C>T
ENST00000698254.1:c.1116C>T	ENSP00000513629.1:p.Phe372=
ENST00000698255.1:c.1536C>T	ENSP00000513630.1:p.Phe512=
ENST00000698256.1:c.1053C>T
ENST00000698257.1:n.1005C>T
ENST00000698258.1:n.722C>T
ENST00000698259.1:n.488C>T
ENST00000265686.8:c.1587C>T MANE Select	ENSP00000265686.3:p.Phe529=
ENST00000265686.7:c.1587C>T	ENSP00000265686.3:p.Phe529=
ENST00000525724.5:n.899C>T
ENST00000528981.5:c.739C>T
ENST00000532635.5:c.939C>T	ENSP00000434407.1:p.Phe313=
ENST00000533005.5:n.700C>T
NM_006019.3:c.1587C>T	NP_006010.2:p.Phe529=
NM_006053.3:c.939C>T	NP_006044.1:p.Phe313=
XM_005273709.2:c.1587C>T	XP_005273766.1:p.Phe529=
XM_011544726.1:c.1587C>T	XP_011543028.1:p.Phe529=
XM_011544727.1:c.1587C>T	XP_011543029.1:p.Phe529=
XM_011544728.1:c.1587C>T	XP_011543030.1:p.Phe529=
XR_949754.1:n.1591C>T
NM_001351059.1:c.693C>T	NP_001337988.1:p.Phe231=
XM_024448320.1:c.1680C>T	XP_024304088.1:p.Phe560=
XM_024448321.1:c.1680C>T	XP_024304089.1:p.Phe560=
XM_024448322.1:c.1680C>T	XP_024304090.1:p.Phe560=
XM_024448323.1:c.1680C>T	XP_024304091.1:p.Phe560=
XM_024448324.1:c.1680C>T	XP_024304092.1:p.Phe560=
XR_001747721.2:n.1711C>T
XR_001747722.1:n.1724C>T
XR_001747723.2:n.1724C>T
XR_002957115.1:n.1802C>T
NM_006019.4:c.1587C>T MANE Select	NP_006010.2:p.Phe529=
NM_001351059.2:c.693C>T	NP_001337988.1:p.Phe231=
NM_006053.4:c.939C>T	NP_006044.1:p.Phe313=