Canonical Allele Identifier: CA381583899

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1855576394
• gnomAD v3: 11-68047725-A-T
• gnomAD v4: 11-68047725-A-T
• MyVariant Identifiers: chr11:g.67815192A>T (hg19) ; chr11:g.68047725A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047725A>T , CM000673.2:g.68047725A>T	GRCh38
NC_000011.9:g.67815192A>T , CM000673.1:g.67815192A>T	GRCh37
NC_000011.8:g.67571768A>T	NCBI36
NG_007878.1:g.13710A>T , LRG_115:g.13710A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.9A>T
ENST00000698254.1:c.913A>T	ENSP00000513629.1:p.Asn305Tyr
ENST00000698255.1:c.1333A>T	ENSP00000513630.1:p.Asn445Tyr
ENST00000698256.1:c.850A>T
ENST00000698257.1:n.802A>T
ENST00000698258.1:n.442A>T
ENST00000698259.1:n.208A>T
ENST00000265686.8:c.1384A>T MANE Select	ENSP00000265686.3:p.Asn462Tyr
ENST00000265686.7:c.1384A>T	ENSP00000265686.3:p.Asn462Tyr
ENST00000525516.1:n.178A>T
ENST00000525724.5:n.696A>T
ENST00000528981.5:c.536A>T
ENST00000529364.1:c.795A>T
ENST00000532635.5:c.736A>T	ENSP00000434407.1:p.Asn246Tyr
ENST00000533005.5:n.420A>T
NM_006019.3:c.1384A>T	NP_006010.2:p.Asn462Tyr
NM_006053.3:c.736A>T	NP_006044.1:p.Asn246Tyr
XM_005273709.2:c.1384A>T	XP_005273766.1:p.Asn462Tyr
XM_011544726.1:c.1384A>T	XP_011543028.1:p.Asn462Tyr
XM_011544727.1:c.1384A>T	XP_011543029.1:p.Asn462Tyr
XM_011544728.1:c.1384A>T	XP_011543030.1:p.Asn462Tyr
XM_011544729.1:c.1400A>T	XP_011543031.1:p.Gln467Leu
XR_949754.1:n.1388A>T
NM_001351059.1:c.490A>T	NP_001337988.1:p.Asn164Tyr
XM_024448320.1:c.1400A>T	XP_024304088.1:p.Gln467Leu
XM_024448321.1:c.1400A>T	XP_024304089.1:p.Gln467Leu
XM_024448322.1:c.1400A>T	XP_024304090.1:p.Gln467Leu
XM_024448323.1:c.1400A>T	XP_024304091.1:p.Gln467Leu
XM_024448324.1:c.1400A>T	XP_024304092.1:p.Gln467Leu
XR_001747721.2:n.1508A>T
XR_001747722.1:n.1521A>T
XR_001747723.2:n.1521A>T
XR_002957115.1:n.1522A>T
NM_006019.4:c.1384A>T MANE Select	NP_006010.2:p.Asn462Tyr
NM_001351059.2:c.490A>T	NP_001337988.1:p.Asn164Tyr
NM_006053.4:c.736A>T	NP_006044.1:p.Asn246Tyr