Canonical Allele Identifier: CA381584255

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1396428560
• gnomAD v2: 11-67815255-A-G
• gnomAD v4: 11-68047788-A-G
• MyVariant Identifiers: chr11:g.67815255A>G (hg19) ; chr11:g.68047788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047788A>G , CM000673.2:g.68047788A>G	GRCh38
NC_000011.9:g.67815255A>G , CM000673.1:g.67815255A>G	GRCh37
NC_000011.8:g.67571831A>G	NCBI36
NG_007878.1:g.13773A>G , LRG_115:g.13773A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.72A>G
ENST00000698254.1:c.976A>G	ENSP00000513629.1:p.Asn326Asp
ENST00000698255.1:c.1396A>G	ENSP00000513630.1:p.Asn466Asp
ENST00000698256.1:c.913A>G
ENST00000698257.1:n.865A>G
ENST00000698258.1:n.505A>G
ENST00000698259.1:n.271A>G
ENST00000265686.8:c.1447A>G MANE Select	ENSP00000265686.3:p.Asn483Asp
ENST00000265686.7:c.1447A>G	ENSP00000265686.3:p.Asn483Asp
ENST00000525516.1:n.241A>G
ENST00000525724.5:n.759A>G
ENST00000528981.5:c.599A>G
ENST00000529364.1:c.858A>G
ENST00000532635.5:c.799A>G	ENSP00000434407.1:p.Asn267Asp
ENST00000533005.5:n.483A>G
NM_006019.3:c.1447A>G	NP_006010.2:p.Asn483Asp
NM_006053.3:c.799A>G	NP_006044.1:p.Asn267Asp
XM_005273709.2:c.1447A>G	XP_005273766.1:p.Asn483Asp
XM_011544726.1:c.1447A>G	XP_011543028.1:p.Asn483Asp
XM_011544727.1:c.1447A>G	XP_011543029.1:p.Asn483Asp
XM_011544728.1:c.1447A>G	XP_011543030.1:p.Asn483Asp
XM_011544729.1:c.1463A>G	XP_011543031.1:p.Gln488Arg
XR_949754.1:n.1451A>G
NM_001351059.1:c.553A>G	NP_001337988.1:p.Asn185Asp
XM_024448320.1:c.1463A>G	XP_024304088.1:p.Gln488Arg
XM_024448321.1:c.1463A>G	XP_024304089.1:p.Gln488Arg
XM_024448322.1:c.1463A>G	XP_024304090.1:p.Gln488Arg
XM_024448323.1:c.1463A>G	XP_024304091.1:p.Gln488Arg
XM_024448324.1:c.1463A>G	XP_024304092.1:p.Gln488Arg
XR_001747721.2:n.1571A>G
XR_001747722.1:n.1584A>G
XR_001747723.2:n.1584A>G
XR_002957115.1:n.1585A>G
NM_006019.4:c.1447A>G MANE Select	NP_006010.2:p.Asn483Asp
NM_001351059.2:c.553A>G	NP_001337988.1:p.Asn185Asp
NM_006053.4:c.799A>G	NP_006044.1:p.Asn267Asp