Canonical Allele Identifier: CA2790247709

Gene: STIM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083748_4083749insACTGAAGAATTCCAGTG , CM000673.2:g.4083748_4083749insACTGAAGAATTCCAGTG	GRCh38
NC_000011.9:g.4104978_4104979insACTGAAGAATTCCAGTG , CM000673.1:g.4104978_4104979insACTGAAGAATTCCAGTG	GRCh37
NC_000011.8:g.4061554_4061555insACTGAAGAATTCCAGTG	NCBI36
NG_016277.1:g.233046_233047insACTGAAGAATTCCAGTG , LRG_164:g.233046_233047insACTGAAGAATTCCAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1252+250_1252+251insACTGAAGAATTCCAGTG	ENSP00000432210.2:n.1252+250_1252+251insACTGAAGAATTCCAGTG
ENST00000698909.1:n.2331+250_2331+251insACTGAAGAATTCCAGTG
ENST00000698910.1:c.985+250_985+251insACTGAAGAATTCCAGTG	ENSP00000514024.1:n.985+250_985+251insACTGAAGAATTCCAGTG
ENST00000698911.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	ENSP00000514025.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
ENST00000698912.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	ENSP00000514026.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
ENST00000698913.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	ENSP00000514027.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
ENST00000698915.1:c.1474+250_1474+251insACTGAAGAATTCCAGTG	ENSP00000514029.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
ENST00000698916.1:c.1495+250_1495+251insACTGAAGAATTCCAGTG	ENSP00000514030.1:n.1495+250_1495+251insACTGAAGAATTCCAGTG
ENST00000698918.1:c.*1175+250_*1175+251insACTGAAGAATTCCAGTG	ENSP00000514031.1:n.*1175+250_*1175+251insACTGAAGAATTCCAGTG
ENST00000698919.1:c.*407+250_*407+251insACTGAAGAATTCCAGTG	ENSP00000514032.1:n.*407+250_*407+251insACTGAAGAATTCCAGTG
ENST00000698920.1:n.774+250_774+251insACTGAAGAATTCCAGTG
ENST00000526596.2:c.1474+250_1474+251insACTGAAGAATTCCAGTG MANE Select	ENSP00000433266.2:n.1474+250_1474+251insACTGAAGAATTCCAGTG
ENST00000300737.8:c.1474+250_1474+251insACTGAAGAATTCCAGTG	ENSP00000300737.4:n.1474+250_1474+251insACTGAAGAATTCCAGTG
ENST00000526596.1:c.666+250_666+251insACTGAAGAATTCCAGTG
ENST00000527651.5:c.1474+250_1474+251insACTGAAGAATTCCAGTG	ENSP00000436208.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
ENST00000531332.1:n.342+250_342+251insACTGAAGAATTCCAGTG
ENST00000533977.5:c.955+250_955+251insACTGAAGAATTCCAGTG	ENSP00000434767.1:n.955+250_955+251insACTGAAGAATTCCAGTG
ENST00000616714.4:c.1474+250_1474+251insACTGAAGAATTCCAGTG	ENSP00000478059.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_001277961.1:c.1474+250_1474+251insACTGAAGAATTCCAGTG	NP_001264890.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_001277962.1:c.1474+250_1474+251insACTGAAGAATTCCAGTG	NP_001264891.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_003156.3:c.1474+250_1474+251insACTGAAGAATTCCAGTG , LRG_164t1:c.1474+250_1474+251insACTGAAGAATTCCAGTG	NP_003147.2:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_001277962.2:c.1474+250_1474+251insACTGAAGAATTCCAGTG	NP_001264891.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_001277961.3:c.1474+250_1474+251insACTGAAGAATTCCAGTG	NP_001264890.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_001382566.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	NP_001369495.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
NM_001382567.1:c.1474+250_1474+251insACTGAAGAATTCCAGTG MANE Select	NP_001369496.1:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NM_001382568.1:c.1495+250_1495+251insACTGAAGAATTCCAGTG	NP_001369497.1:n.1495+250_1495+251insACTGAAGAATTCCAGTG
NM_001382569.1:c.1339+250_1339+251insACTGAAGAATTCCAGTG	NP_001369498.1:n.1339+250_1339+251insACTGAAGAATTCCAGTG
NM_001382570.1:c.1246+250_1246+251insACTGAAGAATTCCAGTG	NP_001369499.1:n.1246+250_1246+251insACTGAAGAATTCCAGTG
NM_001382571.1:c.994+250_994+251insACTGAAGAATTCCAGTG	NP_001369500.1:n.994+250_994+251insACTGAAGAATTCCAGTG
NM_001382575.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	NP_001369504.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
NM_001382576.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	NP_001369505.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
NM_001382577.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	NP_001369506.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
NM_001382578.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	NP_001369507.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
NM_001382579.1:c.1252+250_1252+251insACTGAAGAATTCCAGTG	NP_001369508.1:n.1252+250_1252+251insACTGAAGAATTCCAGTG
NM_001382580.1:c.985+250_985+251insACTGAAGAATTCCAGTG	NP_001369509.1:n.985+250_985+251insACTGAAGAATTCCAGTG
NM_001382581.1:c.985+250_985+251insACTGAAGAATTCCAGTG	NP_001369510.1:n.985+250_985+251insACTGAAGAATTCCAGTG
NM_003156.4:c.1474+250_1474+251insACTGAAGAATTCCAGTG	NP_003147.2:n.1474+250_1474+251insACTGAAGAATTCCAGTG
NR_168436.1:n.1399-2729_1399-2728insACTGAAGAATTCCAGTG
NR_168437.1:n.1903+250_1903+251insACTGAAGAATTCCAGTG
NR_168438.1:n.1725+250_1725+251insACTGAAGAATTCCAGTG