Canonical Allele Identifier: CA381585535

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816446T>A (hg19) ; chr11:g.68048979T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048979T>A , CM000673.2:g.68048979T>A	GRCh38
NC_000011.9:g.67816446T>A , CM000673.1:g.67816446T>A	GRCh37
NC_000011.8:g.67573022T>A	NCBI36
NG_007878.1:g.14964T>A , LRG_115:g.14964T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.280T>A
ENST00000698254.1:c.1184T>A	ENSP00000513629.1:p.Leu395His
ENST00000698255.1:c.1604T>A	ENSP00000513630.1:p.Leu535His
ENST00000698256.1:c.1121T>A
ENST00000698257.1:n.1073T>A
ENST00000698258.1:n.790T>A
ENST00000698259.1:n.556T>A
ENST00000265686.8:c.1655T>A MANE Select	ENSP00000265686.3:p.Leu552His
ENST00000265686.7:c.1655T>A	ENSP00000265686.3:p.Leu552His
ENST00000525724.5:n.967T>A
ENST00000532635.5:c.1007T>A	ENSP00000434407.1:p.Leu336His
ENST00000533005.5:n.768T>A
NM_006019.3:c.1655T>A	NP_006010.2:p.Leu552His
NM_006053.3:c.1007T>A	NP_006044.1:p.Leu336His
XM_005273709.2:c.1655T>A	XP_005273766.1:p.Leu552His
XM_011544726.1:c.1655T>A	XP_011543028.1:p.Leu552His
XM_011544727.1:c.1655T>A	XP_011543029.1:p.Leu552His
XM_011544728.1:c.1655T>A	XP_011543030.1:p.Leu552His
XR_949754.1:n.1659T>A
NM_001351059.1:c.761T>A	NP_001337988.1:p.Leu254His
XM_024448320.1:c.1748T>A	XP_024304088.1:p.Leu583His
XM_024448321.1:c.1748T>A	XP_024304089.1:p.Leu583His
XM_024448322.1:c.1748T>A	XP_024304090.1:p.Leu583His
XM_024448323.1:c.1748T>A	XP_024304091.1:p.Leu583His
XM_024448324.1:c.1748T>A	XP_024304092.1:p.Leu583His
XR_001747721.2:n.1779T>A
XR_001747722.1:n.1792T>A
XR_001747723.2:n.1792T>A
XR_002957115.1:n.1870T>A
NM_006019.4:c.1655T>A MANE Select	NP_006010.2:p.Leu552His
NM_001351059.2:c.761T>A	NP_001337988.1:p.Leu254His
NM_006053.4:c.1007T>A	NP_006044.1:p.Leu336His