Canonical Allele Identifier: CA1948976807
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4083562_4083563delinsGC , CM000673.2:g.4083562_4083563delinsGC GRCh38
NC_000011.9:g.4104792_4104793delinsGC , CM000673.1:g.4104792_4104793delinsGC GRCh37
NC_000011.8:g.4061368_4061369delinsGC NCBI36
NG_016277.1:g.232860_232861delinsGC , LRG_164:g.232860_232861delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.1252+64_1252+65delinsGC ENSP00000432210.2:n.1252+64_1252+65delinsGC
ENST00000533343.2:n.2137_2138delinsGC
ENST00000698909.1:n.2331+64_2331+65delinsGC
ENST00000698910.1:c.985+64_985+65delinsGC ENSP00000514024.1:n.985+64_985+65delinsGC
ENST00000698911.1:c.1252+64_1252+65delinsGC ENSP00000514025.1:n.1252+64_1252+65delinsGC
ENST00000698912.1:c.1252+64_1252+65delinsGC ENSP00000514026.1:n.1252+64_1252+65delinsGC
ENST00000698913.1:c.1252+64_1252+65delinsGC ENSP00000514027.1:n.1252+64_1252+65delinsGC
ENST00000698915.1:c.1474+64_1474+65delinsGC ENSP00000514029.1:n.1474+64_1474+65delinsGC
ENST00000698916.1:c.1495+64_1495+65delinsGC ENSP00000514030.1:n.1495+64_1495+65delinsGC
ENST00000698918.1:c.*1175+64_*1175+65delinsGC ENSP00000514031.1:n.*1175+64_*1175+65delinsGC
ENST00000698919.1:c.*407+64_*407+65delinsGC ENSP00000514032.1:n.*407+64_*407+65delinsGC
ENST00000698920.1:n.774+64_774+65delinsGC
ENST00000526596.2:c.1474+64_1474+65delinsGC MANE Select ENSP00000433266.2:n.1474+64_1474+65delinsGC
ENST00000300737.8:c.1474+64_1474+65delinsGC ENSP00000300737.4:n.1474+64_1474+65delinsGC
ENST00000526596.1:c.666+64_666+65delinsGC
ENST00000527651.5:c.1474+64_1474+65delinsGC ENSP00000436208.1:n.1474+64_1474+65delinsGC
ENST00000531332.1:n.342+64_342+65delinsGC
ENST00000533343.1:n.548_549delinsGC
ENST00000533977.5:c.955+64_955+65delinsGC ENSP00000434767.1:n.955+64_955+65delinsGC
ENST00000616714.4:c.1474+64_1474+65delinsGC ENSP00000478059.1:n.1474+64_1474+65delinsGC
NM_001277961.1:c.1474+64_1474+65delinsGC NP_001264890.1:n.1474+64_1474+65delinsGC
NM_001277962.1:c.1474+64_1474+65delinsGC NP_001264891.1:n.1474+64_1474+65delinsGC
NM_003156.3:c.1474+64_1474+65delinsGC , LRG_164t1:c.1474+64_1474+65delinsGC NP_003147.2:n.1474+64_1474+65delinsGC
NM_001277962.2:c.1474+64_1474+65delinsGC NP_001264891.1:n.1474+64_1474+65delinsGC
NM_001277961.3:c.1474+64_1474+65delinsGC NP_001264890.1:n.1474+64_1474+65delinsGC
NM_001382566.1:c.1252+64_1252+65delinsGC NP_001369495.1:n.1252+64_1252+65delinsGC
NM_001382567.1:c.1474+64_1474+65delinsGC MANE Select NP_001369496.1:n.1474+64_1474+65delinsGC
NM_001382568.1:c.1495+64_1495+65delinsGC NP_001369497.1:n.1495+64_1495+65delinsGC
NM_001382569.1:c.1339+64_1339+65delinsGC NP_001369498.1:n.1339+64_1339+65delinsGC
NM_001382570.1:c.1246+64_1246+65delinsGC NP_001369499.1:n.1246+64_1246+65delinsGC
NM_001382571.1:c.994+64_994+65delinsGC NP_001369500.1:n.994+64_994+65delinsGC
NM_001382573.1:c.*56_*57delinsGC NP_001369502.1:n.*56_*57delinsGC
NM_001382575.1:c.1252+64_1252+65delinsGC NP_001369504.1:n.1252+64_1252+65delinsGC
NM_001382576.1:c.1252+64_1252+65delinsGC NP_001369505.1:n.1252+64_1252+65delinsGC
NM_001382577.1:c.1252+64_1252+65delinsGC NP_001369506.1:n.1252+64_1252+65delinsGC
NM_001382578.1:c.1252+64_1252+65delinsGC NP_001369507.1:n.1252+64_1252+65delinsGC
NM_001382579.1:c.1252+64_1252+65delinsGC NP_001369508.1:n.1252+64_1252+65delinsGC
NM_001382580.1:c.985+64_985+65delinsGC NP_001369509.1:n.985+64_985+65delinsGC
NM_001382581.1:c.985+64_985+65delinsGC NP_001369510.1:n.985+64_985+65delinsGC
NM_003156.4:c.1474+64_1474+65delinsGC NP_003147.2:n.1474+64_1474+65delinsGC
NR_168436.1:n.1399-2915_1399-2914delinsGC
NR_168437.1:n.1903+64_1903+65delinsGC
NR_168438.1:n.1725+64_1725+65delinsGC