Canonical Allele Identifier: CA1948976388
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4083401C= , CM000673.2:g.4083401C= GRCh38
NC_000011.9:g.4104631C= , CM000673.1:g.4104631C= GRCh37
NC_000011.8:g.4061207C= NCBI36
NG_016277.1:g.232699C= , LRG_164:g.232699C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.1155C= ENSP00000432210.2:p.Ser385=
ENST00000533343.2:n.1976C=
ENST00000698909.1:n.2234C=
ENST00000698910.1:c.888C= ENSP00000514024.1:p.Ser296=
ENST00000698911.1:c.1155C= ENSP00000514025.1:p.Ser385=
ENST00000698912.1:c.1155C= ENSP00000514026.1:p.Ser385=
ENST00000698913.1:c.1155C= ENSP00000514027.1:p.Ser385=
ENST00000698915.1:c.1377C= ENSP00000514029.1:p.Ser459=
ENST00000698916.1:c.1398C= ENSP00000514030.1:p.Ser466=
ENST00000698918.1:c.*1078C= ENSP00000514031.1:n.*1078C=
ENST00000698919.1:c.*310C= ENSP00000514032.1:n.*310C=
ENST00000698920.1:n.677C=
ENST00000526596.2:c.1377C= MANE Select ENSP00000433266.2:p.Ser459=
ENST00000300737.8:c.1377C= ENSP00000300737.4:p.Ser459=
ENST00000526596.1:c.569C=
ENST00000527651.5:c.1377C= ENSP00000436208.1:p.Ser459=
ENST00000531332.1:n.245C=
ENST00000533343.1:n.387C=
ENST00000533977.5:c.858C= ENSP00000434767.1:p.Ser286=
ENST00000616714.4:c.1377C= ENSP00000478059.1:p.Ser459=
NM_001277961.1:c.1377C= NP_001264890.1:p.Ser459=
NM_001277962.1:c.1377C= NP_001264891.1:p.Ser459=
NM_003156.3:c.1377C= , LRG_164t1:c.1377C= NP_003147.2:p.Ser459=
NM_001277962.2:c.1377C= NP_001264891.1:p.Ser459=
NM_001277961.3:c.1377C= NP_001264890.1:p.Ser459=
NM_001382566.1:c.1155C= NP_001369495.1:p.Ser385=
NM_001382567.1:c.1377C= MANE Select NP_001369496.1:p.Ser459=
NM_001382568.1:c.1398C= NP_001369497.1:p.Ser466=
NM_001382569.1:c.1242C= NP_001369498.1:p.Ser414=
NM_001382570.1:c.1149C= NP_001369499.1:p.Ser383=
NM_001382571.1:c.897C= NP_001369500.1:p.Ser299=
NM_001382573.1:c.1155C= NP_001369502.1:p.Ser385=
NM_001382575.1:c.1155C= NP_001369504.1:p.Ser385=
NM_001382576.1:c.1155C= NP_001369505.1:p.Ser385=
NM_001382577.1:c.1155C= NP_001369506.1:p.Ser385=
NM_001382578.1:c.1155C= NP_001369507.1:p.Ser385=
NM_001382579.1:c.1155C= NP_001369508.1:p.Ser385=
NM_001382580.1:c.888C= NP_001369509.1:p.Ser296=
NM_001382581.1:c.888C= NP_001369510.1:p.Ser296=
NM_003156.4:c.1377C= NP_003147.2:p.Ser459=
NR_168436.1:n.1399-3076C=
NR_168437.1:n.1806C=
NR_168438.1:n.1628C=