Canonical Allele Identifier: CA381584517

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1455101066
• gnomAD v2: 11-67815380-A-C
• gnomAD v4: 11-68047913-A-C
• MyVariant Identifiers: chr11:g.67815380A>C (hg19) ; chr11:g.68047913A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047913A>C , CM000673.2:g.68047913A>C	GRCh38
NC_000011.9:g.67815380A>C , CM000673.1:g.67815380A>C	GRCh37
NC_000011.8:g.67571956A>C	NCBI36
NG_007878.1:g.13898A>C , LRG_115:g.13898A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.120A>C
ENST00000698254.1:c.1024A>C	ENSP00000513629.1:p.Thr342Pro
ENST00000698255.1:c.1444A>C	ENSP00000513630.1:p.Thr482Pro
ENST00000698256.1:c.961A>C
ENST00000698257.1:n.913A>C
ENST00000698258.1:n.630A>C
ENST00000698259.1:n.396A>C
ENST00000265686.8:c.1495A>C MANE Select	ENSP00000265686.3:p.Thr499Pro
ENST00000265686.7:c.1495A>C	ENSP00000265686.3:p.Thr499Pro
ENST00000525516.1:n.289A>C
ENST00000525724.5:n.807A>C
ENST00000528981.5:c.647A>C
ENST00000532635.5:c.847A>C	ENSP00000434407.1:p.Thr283Pro
ENST00000533005.5:n.608A>C
NM_006019.3:c.1495A>C	NP_006010.2:p.Thr499Pro
NM_006053.3:c.847A>C	NP_006044.1:p.Thr283Pro
XM_005273709.2:c.1495A>C	XP_005273766.1:p.Thr499Pro
XM_011544726.1:c.1495A>C	XP_011543028.1:p.Thr499Pro
XM_011544727.1:c.1495A>C	XP_011543029.1:p.Thr499Pro
XM_011544728.1:c.1495A>C	XP_011543030.1:p.Thr499Pro
XR_949754.1:n.1499A>C
NM_001351059.1:c.601A>C	NP_001337988.1:p.Thr201Pro
XM_024448320.1:c.1588A>C	XP_024304088.1:p.Thr530Pro
XM_024448321.1:c.1588A>C	XP_024304089.1:p.Thr530Pro
XM_024448322.1:c.1588A>C	XP_024304090.1:p.Thr530Pro
XM_024448323.1:c.1588A>C	XP_024304091.1:p.Thr530Pro
XM_024448324.1:c.1588A>C	XP_024304092.1:p.Thr530Pro
XR_001747721.2:n.1619A>C
XR_001747722.1:n.1632A>C
XR_001747723.2:n.1632A>C
XR_002957115.1:n.1710A>C
NM_006019.4:c.1495A>C MANE Select	NP_006010.2:p.Thr499Pro
NM_001351059.2:c.601A>C	NP_001337988.1:p.Thr201Pro
NM_006053.4:c.847A>C	NP_006044.1:p.Thr283Pro