Canonical Allele Identifier: CA1948975870

Gene: STIM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083101_4083102delinsCT , CM000673.2:g.4083101_4083102delinsCT	GRCh38
NC_000011.9:g.4104331_4104332delinsCT , CM000673.1:g.4104331_4104332delinsCT	GRCh37
NC_000011.8:g.4060907_4060908delinsCT	NCBI36
NG_016277.1:g.232399_232400delinsCT , LRG_164:g.232399_232400delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1016+119_1016+120delinsCT	ENSP00000432210.2:n.1016+119_1016+120delinsCT
ENST00000533343.2:n.1837+119_1837+120delinsCT
ENST00000698909.1:n.1934_1935delinsCT
ENST00000698910.1:c.749+119_749+120delinsCT	ENSP00000514024.1:n.749+119_749+120delinsCT
ENST00000698911.1:c.1016+119_1016+120delinsCT	ENSP00000514025.1:n.1016+119_1016+120delinsCT
ENST00000698912.1:c.1016+119_1016+120delinsCT	ENSP00000514026.1:n.1016+119_1016+120delinsCT
ENST00000698913.1:c.1016+119_1016+120delinsCT	ENSP00000514027.1:n.1016+119_1016+120delinsCT
ENST00000698915.1:c.1238+119_1238+120delinsCT	ENSP00000514029.1:n.1238+119_1238+120delinsCT
ENST00000698916.1:c.1259+119_1259+120delinsCT	ENSP00000514030.1:n.1259+119_1259+120delinsCT
ENST00000698918.1:c.*939+119_*939+120delinsCT	ENSP00000514031.1:n.*939+119_*939+120delinsCT
ENST00000698919.1:c.*171+119_*171+120delinsCT	ENSP00000514032.1:n.*171+119_*171+120delinsCT
ENST00000698920.1:n.538+119_538+120delinsCT
ENST00000526596.2:c.1238+119_1238+120delinsCT MANE Select	ENSP00000433266.2:n.1238+119_1238+120delinsCT
ENST00000300737.8:c.1238+119_1238+120delinsCT	ENSP00000300737.4:n.1238+119_1238+120delinsCT
ENST00000526596.1:c.430+119_430+120delinsCT
ENST00000527651.5:c.1238+119_1238+120delinsCT	ENSP00000436208.1:n.1238+119_1238+120delinsCT
ENST00000533343.1:n.248+119_248+120delinsCT
ENST00000533977.5:c.719+119_719+120delinsCT	ENSP00000434767.1:n.719+119_719+120delinsCT
ENST00000616714.4:c.1238+119_1238+120delinsCT	ENSP00000478059.1:n.1238+119_1238+120delinsCT
NM_001277961.1:c.1238+119_1238+120delinsCT	NP_001264890.1:n.1238+119_1238+120delinsCT
NM_001277962.1:c.1238+119_1238+120delinsCT	NP_001264891.1:n.1238+119_1238+120delinsCT
NM_003156.3:c.1238+119_1238+120delinsCT , LRG_164t1:c.1238+119_1238+120delinsCT	NP_003147.2:n.1238+119_1238+120delinsCT
NM_001277962.2:c.1238+119_1238+120delinsCT	NP_001264891.1:n.1238+119_1238+120delinsCT
NM_001277961.3:c.1238+119_1238+120delinsCT	NP_001264890.1:n.1238+119_1238+120delinsCT
NM_001382566.1:c.1016+119_1016+120delinsCT	NP_001369495.1:n.1016+119_1016+120delinsCT
NM_001382567.1:c.1238+119_1238+120delinsCT MANE Select	NP_001369496.1:n.1238+119_1238+120delinsCT
NM_001382568.1:c.1238+119_1238+120delinsCT	NP_001369497.1:n.1238+119_1238+120delinsCT
NM_001382569.1:c.1103+119_1103+120delinsCT	NP_001369498.1:n.1103+119_1103+120delinsCT
NM_001382570.1:c.1010+119_1010+120delinsCT	NP_001369499.1:n.1010+119_1010+120delinsCT
NM_001382571.1:c.758+119_758+120delinsCT	NP_001369500.1:n.758+119_758+120delinsCT
NM_001382573.1:c.1016+119_1016+120delinsCT	NP_001369502.1:n.1016+119_1016+120delinsCT
NM_001382575.1:c.1016+119_1016+120delinsCT	NP_001369504.1:n.1016+119_1016+120delinsCT
NM_001382576.1:c.1016+119_1016+120delinsCT	NP_001369505.1:n.1016+119_1016+120delinsCT
NM_001382577.1:c.1016+119_1016+120delinsCT	NP_001369506.1:n.1016+119_1016+120delinsCT
NM_001382578.1:c.1016+119_1016+120delinsCT	NP_001369507.1:n.1016+119_1016+120delinsCT
NM_001382579.1:c.1016+119_1016+120delinsCT	NP_001369508.1:n.1016+119_1016+120delinsCT
NM_001382580.1:c.749+119_749+120delinsCT	NP_001369509.1:n.749+119_749+120delinsCT
NM_001382581.1:c.749+119_749+120delinsCT	NP_001369510.1:n.749+119_749+120delinsCT
NM_003156.4:c.1238+119_1238+120delinsCT	NP_003147.2:n.1238+119_1238+120delinsCT
NR_168436.1:n.1399-3376_1399-3375delinsCT
NR_168437.1:n.1667+119_1667+120delinsCT
NR_168438.1:n.1489+119_1489+120delinsCT