Canonical Allele Identifier: CA2612107258

Gene: STIM1

Linked Data

• gnomAD v4: 11-4083349-TCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083354_4083356del , CM000673.2:g.4083354_4083356del	GRCh38
NC_000011.9:g.4104584_4104586del , CM000673.1:g.4104584_4104586del	GRCh37
NC_000011.8:g.4061160_4061162del	NCBI36
NG_016277.1:g.232652_232654del , LRG_164:g.232652_232654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1108_1110del	ENSP00000432210.2:p.Asn370del
ENST00000533343.2:n.1929_1931del
ENST00000698909.1:n.2187_2189del
ENST00000698910.1:c.841_843del	ENSP00000514024.1:p.Asn281del
ENST00000698911.1:c.1108_1110del	ENSP00000514025.1:p.Asn370del
ENST00000698912.1:c.1108_1110del	ENSP00000514026.1:p.Asn370del
ENST00000698913.1:c.1108_1110del	ENSP00000514027.1:p.Asn370del
ENST00000698915.1:c.1330_1332del	ENSP00000514029.1:p.Asn444del
ENST00000698916.1:c.1351_1353del	ENSP00000514030.1:p.Asn451del
ENST00000698918.1:c.*1031_*1033del	ENSP00000514031.1:n.*1031_*1033del
ENST00000698919.1:c.*263_*265del	ENSP00000514032.1:n.*263_*265del
ENST00000698920.1:n.630_632del
ENST00000526596.2:c.1330_1332del MANE Select	ENSP00000433266.2:p.Asn444del
ENST00000300737.8:c.1330_1332del	ENSP00000300737.4:p.Asn444del
ENST00000526596.1:c.522_524del
ENST00000527651.5:c.1330_1332del	ENSP00000436208.1:p.Asn444del
ENST00000531332.1:n.198_200del
ENST00000533343.1:n.340_342del
ENST00000533977.5:c.811_813del	ENSP00000434767.1:p.Asn271del
ENST00000616714.4:c.1330_1332del	ENSP00000478059.1:p.Asn444del
NM_001277961.1:c.1330_1332del	NP_001264890.1:p.Asn444del
NM_001277962.1:c.1330_1332del	NP_001264891.1:p.Asn444del
NM_003156.3:c.1330_1332del , LRG_164t1:c.1330_1332del	NP_003147.2:p.Asn444del
NM_001277962.2:c.1330_1332del	NP_001264891.1:p.Asn444del
NM_001277961.3:c.1330_1332del	NP_001264890.1:p.Asn444del
NM_001382566.1:c.1108_1110del	NP_001369495.1:p.Asn370del
NM_001382567.1:c.1330_1332del MANE Select	NP_001369496.1:p.Asn444del
NM_001382568.1:c.1351_1353del	NP_001369497.1:p.Asn451del
NM_001382569.1:c.1195_1197del	NP_001369498.1:p.Asn399del
NM_001382570.1:c.1102_1104del	NP_001369499.1:p.Asn368del
NM_001382571.1:c.850_852del	NP_001369500.1:p.Asn284del
NM_001382573.1:c.1108_1110del	NP_001369502.1:p.Asn370del
NM_001382575.1:c.1108_1110del	NP_001369504.1:p.Asn370del
NM_001382576.1:c.1108_1110del	NP_001369505.1:p.Asn370del
NM_001382577.1:c.1108_1110del	NP_001369506.1:p.Asn370del
NM_001382578.1:c.1108_1110del	NP_001369507.1:p.Asn370del
NM_001382579.1:c.1108_1110del	NP_001369508.1:p.Asn370del
NM_001382580.1:c.841_843del	NP_001369509.1:p.Asn281del
NM_001382581.1:c.841_843del	NP_001369510.1:p.Asn281del
NM_003156.4:c.1330_1332del	NP_003147.2:p.Asn444del
NR_168436.1:n.1399-3123_1399-3121del
NR_168437.1:n.1759_1761del
NR_168438.1:n.1581_1583del