Canonical Allele Identifier: CA1948982422
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4091543C= , CM000673.2:g.4091543C= GRCh38
NC_000011.9:g.4112773C= , CM000673.1:g.4112773C= GRCh37
NC_000011.8:g.4069349C= NCBI36
NG_016277.1:g.240841C= , LRG_164:g.240841C=
NG_027992.2:g.1850C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.*217C= ENSP00000432210.2:n.*217C=
ENST00000698910.1:c.1314C= ENSP00000514024.1:p.Pro438=
ENST00000698911.1:c.1899C= ENSP00000514025.1:p.Pro633=
ENST00000698912.1:c.*217C= ENSP00000514026.1:n.*217C=
ENST00000698913.1:c.1581C= ENSP00000514027.1:p.Pro527=
ENST00000698915.1:c.1887C= ENSP00000514029.1:p.Pro629=
ENST00000698916.1:c.1824C= ENSP00000514030.1:p.Pro608=
ENST00000698918.1:c.*1541C= ENSP00000514031.1:n.*1541C=
ENST00000698919.1:c.*736C= ENSP00000514032.1:n.*736C=
ENST00000698920.1:n.1103C=
ENST00000526596.2:c.1896C= MANE Select ENSP00000433266.2:p.Pro632=
ENST00000300737.8:c.1803C= ENSP00000300737.4:p.Pro601=
ENST00000526156.1:n.601C=
ENST00000526596.1:c.1088C=
ENST00000527651.5:c.*217C= ENSP00000436208.1:n.*217C=
ENST00000533977.5:c.1284C= ENSP00000434767.1:p.Pro428=
ENST00000616714.4:c.2121C= ENSP00000478059.1:p.Pro707=
NM_001277961.1:c.2121C= NP_001264890.1:p.Pro707=
NM_001277962.1:c.*217C= NP_001264891.1:n.*217C=
NM_003156.3:c.1803C= , LRG_164t1:c.1803C= NP_003147.2:p.Pro601=
NM_001277962.2:c.*217C= NP_001264891.1:n.*217C=
NM_001277961.3:c.2121C= NP_001264890.1:p.Pro707=
NM_001382566.1:c.1899C= NP_001369495.1:p.Pro633=
NM_001382567.1:c.1896C= MANE Select NP_001369496.1:p.Pro632=
NM_001382568.1:c.1824C= NP_001369497.1:p.Pro608=
NM_001382569.1:c.1668C= NP_001369498.1:p.Pro556=
NM_001382570.1:c.1575C= NP_001369499.1:p.Pro525=
NM_001382571.1:c.1323C= NP_001369500.1:p.Pro441=
NM_001382575.1:c.1581C= NP_001369504.1:p.Pro527=
NM_001382576.1:c.1581C= NP_001369505.1:p.Pro527=
NM_001382577.1:c.1581C= NP_001369506.1:p.Pro527=
NM_001382578.1:c.*217C= NP_001369507.1:n.*217C=
NM_001382579.1:c.*217C= NP_001369508.1:n.*217C=
NM_001382580.1:c.*217C= NP_001369509.1:n.*217C=
NM_001382581.1:c.1314C= NP_001369510.1:p.Pro438=
NM_003156.4:c.1803C= NP_003147.2:p.Pro601=
NR_168436.1:n.1727C=
NR_168437.1:n.2232C=
NR_168438.1:n.2054C=