Canonical Allele Identifier: CA381583770

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1855574242
• gnomAD v3: 11-68047698-T-G
• gnomAD v4: 11-68047698-T-G
• MyVariant Identifiers: chr11:g.67815165T>G (hg19) ; chr11:g.68047698T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047698T>G , CM000673.2:g.68047698T>G	GRCh38
NC_000011.9:g.67815165T>G , CM000673.1:g.67815165T>G	GRCh37
NC_000011.8:g.67571741T>G	NCBI36
NG_007878.1:g.13683T>G , LRG_115:g.13683T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.886T>G	ENSP00000513629.1:p.Phe296Val
ENST00000698255.1:c.1306T>G	ENSP00000513630.1:p.Phe436Val
ENST00000698256.1:c.823T>G
ENST00000698257.1:n.775T>G
ENST00000698258.1:n.415T>G
ENST00000698259.1:n.181T>G
ENST00000265686.8:c.1357T>G MANE Select	ENSP00000265686.3:p.Phe453Val
ENST00000265686.7:c.1357T>G	ENSP00000265686.3:p.Phe453Val
ENST00000525516.1:n.151T>G
ENST00000525724.5:n.669T>G
ENST00000528981.5:c.509T>G
ENST00000529364.1:c.768T>G
ENST00000532635.5:c.709T>G	ENSP00000434407.1:p.Phe237Val
ENST00000533005.5:n.393T>G
NM_006019.3:c.1357T>G	NP_006010.2:p.Phe453Val
NM_006053.3:c.709T>G	NP_006044.1:p.Phe237Val
XM_005273709.2:c.1357T>G	XP_005273766.1:p.Phe453Val
XM_011544726.1:c.1357T>G	XP_011543028.1:p.Phe453Val
XM_011544727.1:c.1357T>G	XP_011543029.1:p.Phe453Val
XM_011544728.1:c.1357T>G	XP_011543030.1:p.Phe453Val
XM_011544729.1:c.1373T>G	XP_011543031.1:p.Val458Gly
XR_949754.1:n.1361T>G
NM_001351059.1:c.463T>G	NP_001337988.1:p.Phe155Val
XM_024448320.1:c.1373T>G	XP_024304088.1:p.Val458Gly
XM_024448321.1:c.1373T>G	XP_024304089.1:p.Val458Gly
XM_024448322.1:c.1373T>G	XP_024304090.1:p.Val458Gly
XM_024448323.1:c.1373T>G	XP_024304091.1:p.Val458Gly
XM_024448324.1:c.1373T>G	XP_024304092.1:p.Val458Gly
XR_001747721.2:n.1481T>G
XR_001747722.1:n.1494T>G
XR_001747723.2:n.1494T>G
XR_002957115.1:n.1495T>G
NM_006019.4:c.1357T>G MANE Select	NP_006010.2:p.Phe453Val
NM_001351059.2:c.463T>G	NP_001337988.1:p.Phe155Val
NM_006053.4:c.709T>G	NP_006044.1:p.Phe237Val