Canonical Allele Identifier: CA1948982719

Gene: STIM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4092165G= , CM000673.2:g.4092165G=	GRCh38
NC_000011.9:g.4113395G= , CM000673.1:g.4113395G=	GRCh37
NC_000011.8:g.4069971G=	NCBI36
NG_016277.1:g.241463G= , LRG_164:g.241463G=
NG_027992.2:g.2472G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001382567.1:c.*367G= MANE Select	NP_001369496.1:n.*367G=
ENST00000526596.2:c.*367G= MANE Select	ENSP00000433266.2:n.*367G=
NM_001277961.1:c.*367G=	NP_001264890.1:n.*367G=
NM_001277961.3:c.*367G=	NP_001264890.1:n.*367G=
NM_001277962.1:c.*839G=	NP_001264891.1:n.*839G=
NM_001277962.2:c.*839G=	NP_001264891.1:n.*839G=
NM_001382566.1:c.*367G=	NP_001369495.1:n.*367G=
NM_001382568.1:c.*367G=	NP_001369497.1:n.*367G=
NM_001382569.1:c.*367G=	NP_001369498.1:n.*367G=
NM_001382570.1:c.*367G=	NP_001369499.1:n.*367G=
NM_001382571.1:c.*367G=	NP_001369500.1:n.*367G=
NM_001382575.1:c.*367G=	NP_001369504.1:n.*367G=
NM_001382576.1:c.*367G=	NP_001369505.1:n.*367G=
NM_001382577.1:c.*367G=	NP_001369506.1:n.*367G=
NM_001382578.1:c.*839G=	NP_001369507.1:n.*839G=
NM_001382579.1:c.*839G=	NP_001369508.1:n.*839G=
NM_001382580.1:c.*839G=	NP_001369509.1:n.*839G=
NM_001382581.1:c.*367G=	NP_001369510.1:n.*367G=
NM_003156.3:c.*367G= , LRG_164t1:c.*367G=	NP_003147.2:n.*367G=
NM_003156.4:c.*367G=	NP_003147.2:n.*367G=
NR_168436.1:n.2349G=
NR_168437.1:n.2854G=
NR_168438.1:n.2676G=
ENST00000300737.8:c.*367G=	ENSP00000300737.4:n.*367G=
ENST00000525403.6:c.*839G=	ENSP00000432210.2:n.*839G=
ENST00000616714.4:c.*367G=	ENSP00000478059.1:n.*367G=
ENST00000698910.1:c.*367G=	ENSP00000514024.1:n.*367G=
ENST00000698911.1:c.*367G=	ENSP00000514025.1:n.*367G=
ENST00000698912.1:c.*839G=	ENSP00000514026.1:n.*839G=
ENST00000698913.1:c.*367G=	ENSP00000514027.1:n.*367G=
ENST00000698915.1:c.*367G=	ENSP00000514029.1:n.*367G=
ENST00000698916.1:c.*367G=	ENSP00000514030.1:n.*367G=
ENST00000698918.1:c.*2163G=	ENSP00000514031.1:n.*2163G=
ENST00000698919.1:c.*1358G=	ENSP00000514032.1:n.*1358G=
ENST00000698920.1:n.1725G=