Canonical Allele Identifier: CA2740093591

Gene: STIM1

Linked Data

• ClinVar Variation Id: 3061748
• ClinVar RCV Id: RCV003983756

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083477del , CM000673.2:g.4083477del	GRCh38
NC_000011.9:g.4104707del , CM000673.1:g.4104707del	GRCh37
NC_000011.8:g.4061283del	NCBI36
NG_016277.1:g.232775del , LRG_164:g.232775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1231del	ENSP00000432210.2:p.Val411CysfsTer19
ENST00000533343.2:n.2052del
ENST00000698909.1:n.2310del
ENST00000698910.1:c.964del	ENSP00000514024.1:p.Val322CysfsTer19
ENST00000698911.1:c.1231del	ENSP00000514025.1:p.Val411CysfsTer19
ENST00000698912.1:c.1231del	ENSP00000514026.1:p.Val411CysfsTer19
ENST00000698913.1:c.1231del	ENSP00000514027.1:p.Val411CysfsTer19
ENST00000698915.1:c.1453del	ENSP00000514029.1:p.Val485CysfsTer19
ENST00000698916.1:c.1474del	ENSP00000514030.1:p.Val492CysfsTer19
ENST00000698918.1:c.*1154del	ENSP00000514031.1:n.*1154del
ENST00000698919.1:c.*386del	ENSP00000514032.1:n.*386del
ENST00000698920.1:n.753del
ENST00000526596.2:c.1453del MANE Select	ENSP00000433266.2:p.Val485CysfsTer12
ENST00000300737.8:c.1453del	ENSP00000300737.4:p.Val485CysfsTer19
ENST00000526596.1:c.645del
ENST00000527651.5:c.1453del	ENSP00000436208.1:p.Val485CysfsTer19
ENST00000531332.1:n.321del
ENST00000533343.1:n.463del
ENST00000533977.5:c.934del	ENSP00000434767.1:p.Val312CysfsTer19
ENST00000616714.4:c.1453del	ENSP00000478059.1:p.Val485CysfsTer19
NM_001277961.1:c.1453del	NP_001264890.1:p.Val485CysfsTer19
NM_001277962.1:c.1453del	NP_001264891.1:p.Val485CysfsTer19
NM_003156.3:c.1453del , LRG_164t1:c.1453del	NP_003147.2:p.Val485CysfsTer19
NM_001277962.2:c.1453del	NP_001264891.1:p.Val485CysfsTer19
NM_001277961.3:c.1453del	NP_001264890.1:p.Val485CysfsTer19
NM_001382566.1:c.1231del	NP_001369495.1:p.Val411CysfsTer19
NM_001382567.1:c.1453del MANE Select	NP_001369496.1:p.Val485CysfsTer12
NM_001382568.1:c.1474del	NP_001369497.1:p.Val492CysfsTer19
NM_001382569.1:c.1318del	NP_001369498.1:p.Val440CysfsTer19
NM_001382570.1:c.1225del	NP_001369499.1:p.Val409CysfsTer19
NM_001382571.1:c.973del	NP_001369500.1:p.Val325CysfsTer19
NM_001382573.1:c.1231del	NP_001369502.1:p.Val411CysfsTer?
NM_001382575.1:c.1231del	NP_001369504.1:p.Val411CysfsTer19
NM_001382576.1:c.1231del	NP_001369505.1:p.Val411CysfsTer19
NM_001382577.1:c.1231del	NP_001369506.1:p.Val411CysfsTer19
NM_001382578.1:c.1231del	NP_001369507.1:p.Val411CysfsTer19
NM_001382579.1:c.1231del	NP_001369508.1:p.Val411CysfsTer19
NM_001382580.1:c.964del	NP_001369509.1:p.Val322CysfsTer19
NM_001382581.1:c.964del	NP_001369510.1:p.Val322CysfsTer19
NM_003156.4:c.1453del	NP_003147.2:p.Val485CysfsTer19
NR_168436.1:n.1399-3000del
NR_168437.1:n.1882del
NR_168438.1:n.1704del