Canonical Allele Identifier: CA2612107094

Gene: STIM1

Linked Data

• gnomAD v4: 11-4083034-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083034_4083035insC , CM000673.2:g.4083034_4083035insC	GRCh38
NC_000011.9:g.4104264_4104265insC , CM000673.1:g.4104264_4104265insC	GRCh37
NC_000011.8:g.4060840_4060841insC	NCBI36
NG_016277.1:g.232332_232333insC , LRG_164:g.232332_232333insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1016+52_1016+53insC	ENSP00000432210.2:n.1016+52_1016+53insC
ENST00000533343.2:n.1837+52_1837+53insC
ENST00000698909.1:n.1867_1868insC
ENST00000698910.1:c.749+52_749+53insC	ENSP00000514024.1:n.749+52_749+53insC
ENST00000698911.1:c.1016+52_1016+53insC	ENSP00000514025.1:n.1016+52_1016+53insC
ENST00000698912.1:c.1016+52_1016+53insC	ENSP00000514026.1:n.1016+52_1016+53insC
ENST00000698913.1:c.1016+52_1016+53insC	ENSP00000514027.1:n.1016+52_1016+53insC
ENST00000698915.1:c.1238+52_1238+53insC	ENSP00000514029.1:n.1238+52_1238+53insC
ENST00000698916.1:c.1259+52_1259+53insC	ENSP00000514030.1:n.1259+52_1259+53insC
ENST00000698918.1:c.*939+52_*939+53insC	ENSP00000514031.1:n.*939+52_*939+53insC
ENST00000698919.1:c.*171+52_*171+53insC	ENSP00000514032.1:n.*171+52_*171+53insC
ENST00000698920.1:n.538+52_538+53insC
ENST00000526596.2:c.1238+52_1238+53insC MANE Select	ENSP00000433266.2:n.1238+52_1238+53insC
ENST00000300737.8:c.1238+52_1238+53insC	ENSP00000300737.4:n.1238+52_1238+53insC
ENST00000526596.1:c.430+52_430+53insC
ENST00000527651.5:c.1238+52_1238+53insC	ENSP00000436208.1:n.1238+52_1238+53insC
ENST00000533343.1:n.248+52_248+53insC
ENST00000533977.5:c.719+52_719+53insC	ENSP00000434767.1:n.719+52_719+53insC
ENST00000616714.4:c.1238+52_1238+53insC	ENSP00000478059.1:n.1238+52_1238+53insC
NM_001277961.1:c.1238+52_1238+53insC	NP_001264890.1:n.1238+52_1238+53insC
NM_001277962.1:c.1238+52_1238+53insC	NP_001264891.1:n.1238+52_1238+53insC
NM_003156.3:c.1238+52_1238+53insC , LRG_164t1:c.1238+52_1238+53insC	NP_003147.2:n.1238+52_1238+53insC
NM_001277962.2:c.1238+52_1238+53insC	NP_001264891.1:n.1238+52_1238+53insC
NM_001277961.3:c.1238+52_1238+53insC	NP_001264890.1:n.1238+52_1238+53insC
NM_001382566.1:c.1016+52_1016+53insC	NP_001369495.1:n.1016+52_1016+53insC
NM_001382567.1:c.1238+52_1238+53insC MANE Select	NP_001369496.1:n.1238+52_1238+53insC
NM_001382568.1:c.1238+52_1238+53insC	NP_001369497.1:n.1238+52_1238+53insC
NM_001382569.1:c.1103+52_1103+53insC	NP_001369498.1:n.1103+52_1103+53insC
NM_001382570.1:c.1010+52_1010+53insC	NP_001369499.1:n.1010+52_1010+53insC
NM_001382571.1:c.758+52_758+53insC	NP_001369500.1:n.758+52_758+53insC
NM_001382573.1:c.1016+52_1016+53insC	NP_001369502.1:n.1016+52_1016+53insC
NM_001382575.1:c.1016+52_1016+53insC	NP_001369504.1:n.1016+52_1016+53insC
NM_001382576.1:c.1016+52_1016+53insC	NP_001369505.1:n.1016+52_1016+53insC
NM_001382577.1:c.1016+52_1016+53insC	NP_001369506.1:n.1016+52_1016+53insC
NM_001382578.1:c.1016+52_1016+53insC	NP_001369507.1:n.1016+52_1016+53insC
NM_001382579.1:c.1016+52_1016+53insC	NP_001369508.1:n.1016+52_1016+53insC
NM_001382580.1:c.749+52_749+53insC	NP_001369509.1:n.749+52_749+53insC
NM_001382581.1:c.749+52_749+53insC	NP_001369510.1:n.749+52_749+53insC
NM_003156.4:c.1238+52_1238+53insC	NP_003147.2:n.1238+52_1238+53insC
NR_168436.1:n.1399-3443_1399-3442insC
NR_168437.1:n.1667+52_1667+53insC
NR_168438.1:n.1489+52_1489+53insC