Canonical Allele Identifier: CA381584559

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68047925-A-G
• MyVariant Identifiers: chr11:g.67815392A>G (hg19) ; chr11:g.68047925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047925A>G , CM000673.2:g.68047925A>G	GRCh38
NC_000011.9:g.67815392A>G , CM000673.1:g.67815392A>G	GRCh37
NC_000011.8:g.67571968A>G	NCBI36
NG_007878.1:g.13910A>G , LRG_115:g.13910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.132A>G
ENST00000698254.1:c.1036A>G	ENSP00000513629.1:p.Asn346Asp
ENST00000698255.1:c.1456A>G	ENSP00000513630.1:p.Asn486Asp
ENST00000698256.1:c.973A>G
ENST00000698257.1:n.925A>G
ENST00000698258.1:n.642A>G
ENST00000698259.1:n.408A>G
ENST00000265686.8:c.1507A>G MANE Select	ENSP00000265686.3:p.Asn503Asp
ENST00000265686.7:c.1507A>G	ENSP00000265686.3:p.Asn503Asp
ENST00000525516.1:n.301A>G
ENST00000525724.5:n.819A>G
ENST00000528981.5:c.659A>G
ENST00000532635.5:c.859A>G	ENSP00000434407.1:p.Asn287Asp
ENST00000533005.5:n.620A>G
NM_006019.3:c.1507A>G	NP_006010.2:p.Asn503Asp
NM_006053.3:c.859A>G	NP_006044.1:p.Asn287Asp
XM_005273709.2:c.1507A>G	XP_005273766.1:p.Asn503Asp
XM_011544726.1:c.1507A>G	XP_011543028.1:p.Asn503Asp
XM_011544727.1:c.1507A>G	XP_011543029.1:p.Asn503Asp
XM_011544728.1:c.1507A>G	XP_011543030.1:p.Asn503Asp
XR_949754.1:n.1511A>G
NM_001351059.1:c.613A>G	NP_001337988.1:p.Asn205Asp
XM_024448320.1:c.1600A>G	XP_024304088.1:p.Asn534Asp
XM_024448321.1:c.1600A>G	XP_024304089.1:p.Asn534Asp
XM_024448322.1:c.1600A>G	XP_024304090.1:p.Asn534Asp
XM_024448323.1:c.1600A>G	XP_024304091.1:p.Asn534Asp
XM_024448324.1:c.1600A>G	XP_024304092.1:p.Asn534Asp
XR_001747721.2:n.1631A>G
XR_001747722.1:n.1644A>G
XR_001747723.2:n.1644A>G
XR_002957115.1:n.1722A>G
NM_006019.4:c.1507A>G MANE Select	NP_006010.2:p.Asn503Asp
NM_001351059.2:c.613A>G	NP_001337988.1:p.Asn205Asp
NM_006053.4:c.859A>G	NP_006044.1:p.Asn287Asp