Canonical Allele Identifier: CA379197413
Gene: STIM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4091535C>A , CM000673.2:g.4091535C>A GRCh38
NC_000011.9:g.4112765C>A , CM000673.1:g.4112765C>A GRCh37
NC_000011.8:g.4069341C>A NCBI36
NG_016277.1:g.240833C>A , LRG_164:g.240833C>A
NG_027992.2:g.1842C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.*209C>A ENSP00000432210.2:n.*209C>A
ENST00000698910.1:c.1306C>A ENSP00000514024.1:p.Leu436Met
ENST00000698911.1:c.1891C>A ENSP00000514025.1:p.Leu631Met
ENST00000698912.1:c.*209C>A ENSP00000514026.1:n.*209C>A
ENST00000698913.1:c.1573C>A ENSP00000514027.1:p.Leu525Met
ENST00000698915.1:c.1879C>A ENSP00000514029.1:p.Leu627Met
ENST00000698916.1:c.1816C>A ENSP00000514030.1:p.Leu606Met
ENST00000698918.1:c.*1533C>A ENSP00000514031.1:n.*1533C>A
ENST00000698919.1:c.*728C>A ENSP00000514032.1:n.*728C>A
ENST00000698920.1:n.1095C>A
ENST00000526596.2:c.1888C>A MANE Select ENSP00000433266.2:p.Leu630Met
ENST00000300737.8:c.1795C>A ENSP00000300737.4:p.Leu599Met
ENST00000526156.1:n.593C>A
ENST00000526596.1:c.1080C>A
ENST00000527651.5:c.*209C>A ENSP00000436208.1:n.*209C>A
ENST00000533977.5:c.1276C>A ENSP00000434767.1:p.Leu426Met
ENST00000616714.4:c.2113C>A ENSP00000478059.1:p.Leu705Met
NM_001277961.1:c.2113C>A NP_001264890.1:p.Leu705Met
NM_001277962.1:c.*209C>A NP_001264891.1:n.*209C>A
NM_003156.3:c.1795C>A , LRG_164t1:c.1795C>A NP_003147.2:p.Leu599Met
NM_001277962.2:c.*209C>A NP_001264891.1:n.*209C>A
NM_001277961.3:c.2113C>A NP_001264890.1:p.Leu705Met
NM_001382566.1:c.1891C>A NP_001369495.1:p.Leu631Met
NM_001382567.1:c.1888C>A MANE Select NP_001369496.1:p.Leu630Met
NM_001382568.1:c.1816C>A NP_001369497.1:p.Leu606Met
NM_001382569.1:c.1660C>A NP_001369498.1:p.Leu554Met
NM_001382570.1:c.1567C>A NP_001369499.1:p.Leu523Met
NM_001382571.1:c.1315C>A NP_001369500.1:p.Leu439Met
NM_001382575.1:c.1573C>A NP_001369504.1:p.Leu525Met
NM_001382576.1:c.1573C>A NP_001369505.1:p.Leu525Met
NM_001382577.1:c.1573C>A NP_001369506.1:p.Leu525Met
NM_001382578.1:c.*209C>A NP_001369507.1:n.*209C>A
NM_001382579.1:c.*209C>A NP_001369508.1:n.*209C>A
NM_001382580.1:c.*209C>A NP_001369509.1:n.*209C>A
NM_001382581.1:c.1306C>A NP_001369510.1:p.Leu436Met
NM_003156.4:c.1795C>A NP_003147.2:p.Leu599Met
NR_168436.1:n.1719C>A
NR_168437.1:n.2224C>A
NR_168438.1:n.2046C>A