Canonical Allele Identifier: CA1948976171
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4083315C= , CM000673.2:g.4083315C= GRCh38
NC_000011.9:g.4104545C= , CM000673.1:g.4104545C= GRCh37
NC_000011.8:g.4061121C= NCBI36
NG_016277.1:g.232613C= , LRG_164:g.232613C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.1069C= ENSP00000432210.2:p.Gln357=
ENST00000533343.2:n.1890C=
ENST00000698909.1:n.2148C=
ENST00000698910.1:c.802C= ENSP00000514024.1:p.Gln268=
ENST00000698911.1:c.1069C= ENSP00000514025.1:p.Gln357=
ENST00000698912.1:c.1069C= ENSP00000514026.1:p.Gln357=
ENST00000698913.1:c.1069C= ENSP00000514027.1:p.Gln357=
ENST00000698915.1:c.1291C= ENSP00000514029.1:p.Gln431=
ENST00000698916.1:c.1312C= ENSP00000514030.1:p.Gln438=
ENST00000698918.1:c.*992C= ENSP00000514031.1:n.*992C=
ENST00000698919.1:c.*224C= ENSP00000514032.1:n.*224C=
ENST00000698920.1:n.591C=
ENST00000526596.2:c.1291C= MANE Select ENSP00000433266.2:p.Gln431=
ENST00000300737.8:c.1291C= ENSP00000300737.4:p.Gln431=
ENST00000526596.1:c.483C=
ENST00000527651.5:c.1291C= ENSP00000436208.1:p.Gln431=
ENST00000531332.1:n.159C=
ENST00000533343.1:n.301C=
ENST00000533977.5:c.772C= ENSP00000434767.1:p.Gln258=
ENST00000616714.4:c.1291C= ENSP00000478059.1:p.Gln431=
NM_001277961.1:c.1291C= NP_001264890.1:p.Gln431=
NM_001277962.1:c.1291C= NP_001264891.1:p.Gln431=
NM_003156.3:c.1291C= , LRG_164t1:c.1291C= NP_003147.2:p.Gln431=
NM_001277962.2:c.1291C= NP_001264891.1:p.Gln431=
NM_001277961.3:c.1291C= NP_001264890.1:p.Gln431=
NM_001382566.1:c.1069C= NP_001369495.1:p.Gln357=
NM_001382567.1:c.1291C= MANE Select NP_001369496.1:p.Gln431=
NM_001382568.1:c.1312C= NP_001369497.1:p.Gln438=
NM_001382569.1:c.1156C= NP_001369498.1:p.Gln386=
NM_001382570.1:c.1063C= NP_001369499.1:p.Gln355=
NM_001382571.1:c.811C= NP_001369500.1:p.Gln271=
NM_001382573.1:c.1069C= NP_001369502.1:p.Gln357=
NM_001382575.1:c.1069C= NP_001369504.1:p.Gln357=
NM_001382576.1:c.1069C= NP_001369505.1:p.Gln357=
NM_001382577.1:c.1069C= NP_001369506.1:p.Gln357=
NM_001382578.1:c.1069C= NP_001369507.1:p.Gln357=
NM_001382579.1:c.1069C= NP_001369508.1:p.Gln357=
NM_001382580.1:c.802C= NP_001369509.1:p.Gln268=
NM_001382581.1:c.802C= NP_001369510.1:p.Gln268=
NM_003156.4:c.1291C= NP_003147.2:p.Gln431=
NR_168436.1:n.1399-3162C=
NR_168437.1:n.1720C=
NR_168438.1:n.1542C=