Canonical Allele Identifier: CA1948976799

Gene: STIM1

Linked Data

• dbSNP Id: rs762909859

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083545A>T , CM000673.2:g.4083545A>T	GRCh38
NC_000011.9:g.4104775A>T , CM000673.1:g.4104775A>T	GRCh37
NC_000011.8:g.4061351A>T	NCBI36
NG_016277.1:g.232843A>T , LRG_164:g.232843A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1252+47A>T	ENSP00000432210.2:n.1252+47A>T
ENST00000533343.2:n.2120A>T
ENST00000698909.1:n.2331+47A>T
ENST00000698910.1:c.985+47A>T	ENSP00000514024.1:n.985+47A>T
ENST00000698911.1:c.1252+47A>T	ENSP00000514025.1:n.1252+47A>T
ENST00000698912.1:c.1252+47A>T	ENSP00000514026.1:n.1252+47A>T
ENST00000698913.1:c.1252+47A>T	ENSP00000514027.1:n.1252+47A>T
ENST00000698915.1:c.1474+47A>T	ENSP00000514029.1:n.1474+47A>T
ENST00000698916.1:c.1495+47A>T	ENSP00000514030.1:n.1495+47A>T
ENST00000698918.1:c.*1175+47A>T	ENSP00000514031.1:n.*1175+47A>T
ENST00000698919.1:c.*407+47A>T	ENSP00000514032.1:n.*407+47A>T
ENST00000698920.1:n.774+47A>T
ENST00000526596.2:c.1474+47A>T MANE Select	ENSP00000433266.2:n.1474+47A>T
ENST00000300737.8:c.1474+47A>T	ENSP00000300737.4:n.1474+47A>T
ENST00000526596.1:c.666+47A>T
ENST00000527651.5:c.1474+47A>T	ENSP00000436208.1:n.1474+47A>T
ENST00000531332.1:n.342+47A>T
ENST00000533343.1:n.531A>T
ENST00000533977.5:c.955+47A>T	ENSP00000434767.1:n.955+47A>T
ENST00000616714.4:c.1474+47A>T	ENSP00000478059.1:n.1474+47A>T
NM_001277961.1:c.1474+47A>T	NP_001264890.1:n.1474+47A>T
NM_001277962.1:c.1474+47A>T	NP_001264891.1:n.1474+47A>T
NM_003156.3:c.1474+47A>T , LRG_164t1:c.1474+47A>T	NP_003147.2:n.1474+47A>T
NM_001277962.2:c.1474+47A>T	NP_001264891.1:n.1474+47A>T
NM_001277961.3:c.1474+47A>T	NP_001264890.1:n.1474+47A>T
NM_001382566.1:c.1252+47A>T	NP_001369495.1:n.1252+47A>T
NM_001382567.1:c.1474+47A>T MANE Select	NP_001369496.1:n.1474+47A>T
NM_001382568.1:c.1495+47A>T	NP_001369497.1:n.1495+47A>T
NM_001382569.1:c.1339+47A>T	NP_001369498.1:n.1339+47A>T
NM_001382570.1:c.1246+47A>T	NP_001369499.1:n.1246+47A>T
NM_001382571.1:c.994+47A>T	NP_001369500.1:n.994+47A>T
NM_001382573.1:c.*39A>T	NP_001369502.1:n.*39A>T
NM_001382575.1:c.1252+47A>T	NP_001369504.1:n.1252+47A>T
NM_001382576.1:c.1252+47A>T	NP_001369505.1:n.1252+47A>T
NM_001382577.1:c.1252+47A>T	NP_001369506.1:n.1252+47A>T
NM_001382578.1:c.1252+47A>T	NP_001369507.1:n.1252+47A>T
NM_001382579.1:c.1252+47A>T	NP_001369508.1:n.1252+47A>T
NM_001382580.1:c.985+47A>T	NP_001369509.1:n.985+47A>T
NM_001382581.1:c.985+47A>T	NP_001369510.1:n.985+47A>T
NM_003156.4:c.1474+47A>T	NP_003147.2:n.1474+47A>T
NR_168436.1:n.1399-2932A>T
NR_168437.1:n.1903+47A>T
NR_168438.1:n.1725+47A>T