Canonical Allele Identifier: CA1948975762

Gene: STIM1

Linked Data

• dbSNP Id: rs2094473427
• gnomAD v4: 11-4083019-TATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083023_4083025del , CM000673.2:g.4083023_4083025del	GRCh38
NC_000011.9:g.4104253_4104255del , CM000673.1:g.4104253_4104255del	GRCh37
NC_000011.8:g.4060829_4060831del	NCBI36
NG_016277.1:g.232321_232323del , LRG_164:g.232321_232323del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1016+41_1016+43del	ENSP00000432210.2:n.1016+41_1016+43del
ENST00000533343.2:n.1837+41_1837+43del
ENST00000698909.1:n.1856_1858del
ENST00000698910.1:c.749+41_749+43del	ENSP00000514024.1:n.749+41_749+43del
ENST00000698911.1:c.1016+41_1016+43del	ENSP00000514025.1:n.1016+41_1016+43del
ENST00000698912.1:c.1016+41_1016+43del	ENSP00000514026.1:n.1016+41_1016+43del
ENST00000698913.1:c.1016+41_1016+43del	ENSP00000514027.1:n.1016+41_1016+43del
ENST00000698915.1:c.1238+41_1238+43del	ENSP00000514029.1:n.1238+41_1238+43del
ENST00000698916.1:c.1259+41_1259+43del	ENSP00000514030.1:n.1259+41_1259+43del
ENST00000698918.1:c.*939+41_*939+43del	ENSP00000514031.1:n.*939+41_*939+43del
ENST00000698919.1:c.*171+41_*171+43del	ENSP00000514032.1:n.*171+41_*171+43del
ENST00000698920.1:n.538+41_538+43del
ENST00000526596.2:c.1238+41_1238+43del MANE Select	ENSP00000433266.2:n.1238+41_1238+43del
ENST00000300737.8:c.1238+41_1238+43del	ENSP00000300737.4:n.1238+41_1238+43del
ENST00000526596.1:c.430+41_430+43del
ENST00000527651.5:c.1238+41_1238+43del	ENSP00000436208.1:n.1238+41_1238+43del
ENST00000533343.1:n.248+41_248+43del
ENST00000533977.5:c.719+41_719+43del	ENSP00000434767.1:n.719+41_719+43del
ENST00000616714.4:c.1238+41_1238+43del	ENSP00000478059.1:n.1238+41_1238+43del
NM_001277961.1:c.1238+41_1238+43del	NP_001264890.1:n.1238+41_1238+43del
NM_001277962.1:c.1238+41_1238+43del	NP_001264891.1:n.1238+41_1238+43del
NM_003156.3:c.1238+41_1238+43del , LRG_164t1:c.1238+41_1238+43del	NP_003147.2:n.1238+41_1238+43del
NM_001277962.2:c.1238+41_1238+43del	NP_001264891.1:n.1238+41_1238+43del
NM_001277961.3:c.1238+41_1238+43del	NP_001264890.1:n.1238+41_1238+43del
NM_001382566.1:c.1016+41_1016+43del	NP_001369495.1:n.1016+41_1016+43del
NM_001382567.1:c.1238+41_1238+43del MANE Select	NP_001369496.1:n.1238+41_1238+43del
NM_001382568.1:c.1238+41_1238+43del	NP_001369497.1:n.1238+41_1238+43del
NM_001382569.1:c.1103+41_1103+43del	NP_001369498.1:n.1103+41_1103+43del
NM_001382570.1:c.1010+41_1010+43del	NP_001369499.1:n.1010+41_1010+43del
NM_001382571.1:c.758+41_758+43del	NP_001369500.1:n.758+41_758+43del
NM_001382573.1:c.1016+41_1016+43del	NP_001369502.1:n.1016+41_1016+43del
NM_001382575.1:c.1016+41_1016+43del	NP_001369504.1:n.1016+41_1016+43del
NM_001382576.1:c.1016+41_1016+43del	NP_001369505.1:n.1016+41_1016+43del
NM_001382577.1:c.1016+41_1016+43del	NP_001369506.1:n.1016+41_1016+43del
NM_001382578.1:c.1016+41_1016+43del	NP_001369507.1:n.1016+41_1016+43del
NM_001382579.1:c.1016+41_1016+43del	NP_001369508.1:n.1016+41_1016+43del
NM_001382580.1:c.749+41_749+43del	NP_001369509.1:n.749+41_749+43del
NM_001382581.1:c.749+41_749+43del	NP_001369510.1:n.749+41_749+43del
NM_003156.4:c.1238+41_1238+43del	NP_003147.2:n.1238+41_1238+43del
NR_168436.1:n.1399-3454_1399-3452del
NR_168437.1:n.1667+41_1667+43del
NR_168438.1:n.1489+41_1489+43del