Canonical Allele Identifier: CA381585087

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816388T>A (hg19) ; chr11:g.68048921T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048921T>A , CM000673.2:g.68048921T>A	GRCh38
NC_000011.9:g.67816388T>A , CM000673.1:g.67816388T>A	GRCh37
NC_000011.8:g.67572964T>A	NCBI36
NG_007878.1:g.14906T>A , LRG_115:g.14906T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.222T>A
ENST00000698254.1:c.1126T>A	ENSP00000513629.1:p.Phe376Ile
ENST00000698255.1:c.1546T>A	ENSP00000513630.1:p.Phe516Ile
ENST00000698256.1:c.1063T>A
ENST00000698257.1:n.1015T>A
ENST00000698258.1:n.732T>A
ENST00000698259.1:n.498T>A
ENST00000265686.8:c.1597T>A MANE Select	ENSP00000265686.3:p.Phe533Ile
ENST00000265686.7:c.1597T>A	ENSP00000265686.3:p.Phe533Ile
ENST00000525724.5:n.909T>A
ENST00000528981.5:c.749T>A
ENST00000532635.5:c.949T>A	ENSP00000434407.1:p.Phe317Ile
ENST00000533005.5:n.710T>A
NM_006019.3:c.1597T>A	NP_006010.2:p.Phe533Ile
NM_006053.3:c.949T>A	NP_006044.1:p.Phe317Ile
XM_005273709.2:c.1597T>A	XP_005273766.1:p.Phe533Ile
XM_011544726.1:c.1597T>A	XP_011543028.1:p.Phe533Ile
XM_011544727.1:c.1597T>A	XP_011543029.1:p.Phe533Ile
XM_011544728.1:c.1597T>A	XP_011543030.1:p.Phe533Ile
XR_949754.1:n.1601T>A
NM_001351059.1:c.703T>A	NP_001337988.1:p.Phe235Ile
XM_024448320.1:c.1690T>A	XP_024304088.1:p.Phe564Ile
XM_024448321.1:c.1690T>A	XP_024304089.1:p.Phe564Ile
XM_024448322.1:c.1690T>A	XP_024304090.1:p.Phe564Ile
XM_024448323.1:c.1690T>A	XP_024304091.1:p.Phe564Ile
XM_024448324.1:c.1690T>A	XP_024304092.1:p.Phe564Ile
XR_001747721.2:n.1721T>A
XR_001747722.1:n.1734T>A
XR_001747723.2:n.1734T>A
XR_002957115.1:n.1812T>A
NM_006019.4:c.1597T>A MANE Select	NP_006010.2:p.Phe533Ile
NM_001351059.2:c.703T>A	NP_001337988.1:p.Phe235Ile
NM_006053.4:c.949T>A	NP_006044.1:p.Phe317Ile