Canonical Allele Identifier: CA381584436

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815356T>G (hg19) ; chr11:g.68047889T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047889T>G , CM000673.2:g.68047889T>G	GRCh38
NC_000011.9:g.67815356T>G , CM000673.1:g.67815356T>G	GRCh37
NC_000011.8:g.67571932T>G	NCBI36
NG_007878.1:g.13874T>G , LRG_115:g.13874T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.96T>G
ENST00000698254.1:c.1000T>G	ENSP00000513629.1:p.Phe334Val
ENST00000698255.1:c.1420T>G	ENSP00000513630.1:p.Phe474Val
ENST00000698256.1:c.937T>G
ENST00000698257.1:n.889T>G
ENST00000698258.1:n.606T>G
ENST00000698259.1:n.372T>G
ENST00000265686.8:c.1471T>G MANE Select	ENSP00000265686.3:p.Phe491Val
ENST00000265686.7:c.1471T>G	ENSP00000265686.3:p.Phe491Val
ENST00000525516.1:n.265T>G
ENST00000525724.5:n.783T>G
ENST00000528981.5:c.623T>G
ENST00000532635.5:c.823T>G	ENSP00000434407.1:p.Phe275Val
ENST00000533005.5:n.584T>G
NM_006019.3:c.1471T>G	NP_006010.2:p.Phe491Val
NM_006053.3:c.823T>G	NP_006044.1:p.Phe275Val
XM_005273709.2:c.1471T>G	XP_005273766.1:p.Phe491Val
XM_011544726.1:c.1471T>G	XP_011543028.1:p.Phe491Val
XM_011544727.1:c.1471T>G	XP_011543029.1:p.Phe491Val
XM_011544728.1:c.1471T>G	XP_011543030.1:p.Phe491Val
XM_011544729.1:c.*5T>G	XP_011543031.1:n.*5T>G
XR_949754.1:n.1475T>G
NM_001351059.1:c.577T>G	NP_001337988.1:p.Phe193Val
XM_024448320.1:c.1564T>G	XP_024304088.1:p.Phe522Val
XM_024448321.1:c.1564T>G	XP_024304089.1:p.Phe522Val
XM_024448322.1:c.1564T>G	XP_024304090.1:p.Phe522Val
XM_024448323.1:c.1564T>G	XP_024304091.1:p.Phe522Val
XM_024448324.1:c.1564T>G	XP_024304092.1:p.Phe522Val
XR_001747721.2:n.1595T>G
XR_001747722.1:n.1608T>G
XR_001747723.2:n.1608T>G
XR_002957115.1:n.1686T>G
NM_006019.4:c.1471T>G MANE Select	NP_006010.2:p.Phe491Val
NM_001351059.2:c.577T>G	NP_001337988.1:p.Phe193Val
NM_006053.4:c.823T>G	NP_006044.1:p.Phe275Val