Canonical Allele Identifier: CA381585027

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816378C>G (hg19) ; chr11:g.68048911C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.212C>G
ENST00000698254.1:c.1116C>G	ENSP00000513629.1:p.Phe372Leu
ENST00000698255.1:c.1536C>G	ENSP00000513630.1:p.Phe512Leu
ENST00000698256.1:c.1053C>G
ENST00000698257.1:n.1005C>G
ENST00000698258.1:n.722C>G
ENST00000698259.1:n.488C>G
ENST00000265686.8:c.1587C>G MANE Select	ENSP00000265686.3:p.Phe529Leu
ENST00000265686.7:c.1587C>G	ENSP00000265686.3:p.Phe529Leu
ENST00000525724.5:n.899C>G
ENST00000528981.5:c.739C>G
ENST00000532635.5:c.939C>G	ENSP00000434407.1:p.Phe313Leu
ENST00000533005.5:n.700C>G
NM_006019.3:c.1587C>G	NP_006010.2:p.Phe529Leu
NM_006053.3:c.939C>G	NP_006044.1:p.Phe313Leu
XM_005273709.2:c.1587C>G	XP_005273766.1:p.Phe529Leu
XM_011544726.1:c.1587C>G	XP_011543028.1:p.Phe529Leu
XM_011544727.1:c.1587C>G	XP_011543029.1:p.Phe529Leu
XM_011544728.1:c.1587C>G	XP_011543030.1:p.Phe529Leu
XR_949754.1:n.1591C>G
NM_001351059.1:c.693C>G	NP_001337988.1:p.Phe231Leu
XM_024448320.1:c.1680C>G	XP_024304088.1:p.Phe560Leu
XM_024448321.1:c.1680C>G	XP_024304089.1:p.Phe560Leu
XM_024448322.1:c.1680C>G	XP_024304090.1:p.Phe560Leu
XM_024448323.1:c.1680C>G	XP_024304091.1:p.Phe560Leu
XM_024448324.1:c.1680C>G	XP_024304092.1:p.Phe560Leu
XR_001747721.2:n.1711C>G
XR_001747722.1:n.1724C>G
XR_001747723.2:n.1724C>G
XR_002957115.1:n.1802C>G
NM_006019.4:c.1587C>G MANE Select	NP_006010.2:p.Phe529Leu
NM_001351059.2:c.693C>G	NP_001337988.1:p.Phe231Leu
NM_006053.4:c.939C>G	NP_006044.1:p.Phe313Leu