Canonical Allele Identifier: CA379197522
Gene: STIM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4091563C>A , CM000673.2:g.4091563C>A GRCh38
NC_000011.9:g.4112793C>A , CM000673.1:g.4112793C>A GRCh37
NC_000011.8:g.4069369C>A NCBI36
NG_016277.1:g.240861C>A , LRG_164:g.240861C>A
NG_027992.2:g.1870C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.*237C>A ENSP00000432210.2:n.*237C>A
ENST00000698910.1:c.1334C>A ENSP00000514024.1:p.Ser445Tyr
ENST00000698911.1:c.1919C>A ENSP00000514025.1:p.Ser640Tyr
ENST00000698912.1:c.*237C>A ENSP00000514026.1:n.*237C>A
ENST00000698913.1:c.1601C>A ENSP00000514027.1:p.Ser534Tyr
ENST00000698915.1:c.1907C>A ENSP00000514029.1:p.Ser636Tyr
ENST00000698916.1:c.1844C>A ENSP00000514030.1:p.Ser615Tyr
ENST00000698918.1:c.*1561C>A ENSP00000514031.1:n.*1561C>A
ENST00000698919.1:c.*756C>A ENSP00000514032.1:n.*756C>A
ENST00000698920.1:n.1123C>A
ENST00000526596.2:c.1916C>A MANE Select ENSP00000433266.2:p.Ser639Tyr
ENST00000300737.8:c.1823C>A ENSP00000300737.4:p.Ser608Tyr
ENST00000526156.1:n.621C>A
ENST00000526596.1:c.1108C>A
ENST00000527651.5:c.*237C>A ENSP00000436208.1:n.*237C>A
ENST00000533977.5:c.1304C>A ENSP00000434767.1:p.Ser435Tyr
ENST00000616714.4:c.2141C>A ENSP00000478059.1:p.Ser714Tyr
NM_001277961.1:c.2141C>A NP_001264890.1:p.Ser714Tyr
NM_001277962.1:c.*237C>A NP_001264891.1:n.*237C>A
NM_003156.3:c.1823C>A , LRG_164t1:c.1823C>A NP_003147.2:p.Ser608Tyr
NM_001277962.2:c.*237C>A NP_001264891.1:n.*237C>A
NM_001277961.3:c.2141C>A NP_001264890.1:p.Ser714Tyr
NM_001382566.1:c.1919C>A NP_001369495.1:p.Ser640Tyr
NM_001382567.1:c.1916C>A MANE Select NP_001369496.1:p.Ser639Tyr
NM_001382568.1:c.1844C>A NP_001369497.1:p.Ser615Tyr
NM_001382569.1:c.1688C>A NP_001369498.1:p.Ser563Tyr
NM_001382570.1:c.1595C>A NP_001369499.1:p.Ser532Tyr
NM_001382571.1:c.1343C>A NP_001369500.1:p.Ser448Tyr
NM_001382575.1:c.1601C>A NP_001369504.1:p.Ser534Tyr
NM_001382576.1:c.1601C>A NP_001369505.1:p.Ser534Tyr
NM_001382577.1:c.1601C>A NP_001369506.1:p.Ser534Tyr
NM_001382578.1:c.*237C>A NP_001369507.1:n.*237C>A
NM_001382579.1:c.*237C>A NP_001369508.1:n.*237C>A
NM_001382580.1:c.*237C>A NP_001369509.1:n.*237C>A
NM_001382581.1:c.1334C>A NP_001369510.1:p.Ser445Tyr
NM_003156.4:c.1823C>A NP_003147.2:p.Ser608Tyr
NR_168436.1:n.1747C>A
NR_168437.1:n.2252C>A
NR_168438.1:n.2074C>A