Canonical Allele Identifier: CA1948976870
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4083670_4083671delinsTC , CM000673.2:g.4083670_4083671delinsTC GRCh38
NC_000011.9:g.4104900_4104901delinsTC , CM000673.1:g.4104900_4104901delinsTC GRCh37
NC_000011.8:g.4061476_4061477delinsTC NCBI36
NG_016277.1:g.232968_232969delinsTC , LRG_164:g.232968_232969delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.1252+172_1252+173delinsTC ENSP00000432210.2:n.1252+172_1252+173delinsTC
ENST00000698909.1:n.2331+172_2331+173delinsTC
ENST00000698910.1:c.985+172_985+173delinsTC ENSP00000514024.1:n.985+172_985+173delinsTC
ENST00000698911.1:c.1252+172_1252+173delinsTC ENSP00000514025.1:n.1252+172_1252+173delinsTC
ENST00000698912.1:c.1252+172_1252+173delinsTC ENSP00000514026.1:n.1252+172_1252+173delinsTC
ENST00000698913.1:c.1252+172_1252+173delinsTC ENSP00000514027.1:n.1252+172_1252+173delinsTC
ENST00000698915.1:c.1474+172_1474+173delinsTC ENSP00000514029.1:n.1474+172_1474+173delinsTC
ENST00000698916.1:c.1495+172_1495+173delinsTC ENSP00000514030.1:n.1495+172_1495+173delinsTC
ENST00000698918.1:c.*1175+172_*1175+173delinsTC ENSP00000514031.1:n.*1175+172_*1175+173delinsTC
ENST00000698919.1:c.*407+172_*407+173delinsTC ENSP00000514032.1:n.*407+172_*407+173delinsTC
ENST00000698920.1:n.774+172_774+173delinsTC
ENST00000526596.2:c.1474+172_1474+173delinsTC MANE Select ENSP00000433266.2:n.1474+172_1474+173delinsTC
ENST00000300737.8:c.1474+172_1474+173delinsTC ENSP00000300737.4:n.1474+172_1474+173delinsTC
ENST00000526596.1:c.666+172_666+173delinsTC
ENST00000527651.5:c.1474+172_1474+173delinsTC ENSP00000436208.1:n.1474+172_1474+173delinsTC
ENST00000531332.1:n.342+172_342+173delinsTC
ENST00000533977.5:c.955+172_955+173delinsTC ENSP00000434767.1:n.955+172_955+173delinsTC
ENST00000616714.4:c.1474+172_1474+173delinsTC ENSP00000478059.1:n.1474+172_1474+173delinsTC
NM_001277961.1:c.1474+172_1474+173delinsTC NP_001264890.1:n.1474+172_1474+173delinsTC
NM_001277962.1:c.1474+172_1474+173delinsTC NP_001264891.1:n.1474+172_1474+173delinsTC
NM_003156.3:c.1474+172_1474+173delinsTC , LRG_164t1:c.1474+172_1474+173delinsTC NP_003147.2:n.1474+172_1474+173delinsTC
NM_001277962.2:c.1474+172_1474+173delinsTC NP_001264891.1:n.1474+172_1474+173delinsTC
NM_001277961.3:c.1474+172_1474+173delinsTC NP_001264890.1:n.1474+172_1474+173delinsTC
NM_001382566.1:c.1252+172_1252+173delinsTC NP_001369495.1:n.1252+172_1252+173delinsTC
NM_001382567.1:c.1474+172_1474+173delinsTC MANE Select NP_001369496.1:n.1474+172_1474+173delinsTC
NM_001382568.1:c.1495+172_1495+173delinsTC NP_001369497.1:n.1495+172_1495+173delinsTC
NM_001382569.1:c.1339+172_1339+173delinsTC NP_001369498.1:n.1339+172_1339+173delinsTC
NM_001382570.1:c.1246+172_1246+173delinsTC NP_001369499.1:n.1246+172_1246+173delinsTC
NM_001382571.1:c.994+172_994+173delinsTC NP_001369500.1:n.994+172_994+173delinsTC
NM_001382575.1:c.1252+172_1252+173delinsTC NP_001369504.1:n.1252+172_1252+173delinsTC
NM_001382576.1:c.1252+172_1252+173delinsTC NP_001369505.1:n.1252+172_1252+173delinsTC
NM_001382577.1:c.1252+172_1252+173delinsTC NP_001369506.1:n.1252+172_1252+173delinsTC
NM_001382578.1:c.1252+172_1252+173delinsTC NP_001369507.1:n.1252+172_1252+173delinsTC
NM_001382579.1:c.1252+172_1252+173delinsTC NP_001369508.1:n.1252+172_1252+173delinsTC
NM_001382580.1:c.985+172_985+173delinsTC NP_001369509.1:n.985+172_985+173delinsTC
NM_001382581.1:c.985+172_985+173delinsTC NP_001369510.1:n.985+172_985+173delinsTC
NM_003156.4:c.1474+172_1474+173delinsTC NP_003147.2:n.1474+172_1474+173delinsTC
NR_168436.1:n.1399-2807_1399-2806delinsTC
NR_168437.1:n.1903+172_1903+173delinsTC
NR_168438.1:n.1725+172_1725+173delinsTC