Canonical Allele Identifier: CA379197438

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112770C>G (hg19) ; chr11:g.4091540C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091540C>G , CM000673.2:g.4091540C>G	GRCh38
NC_000011.9:g.4112770C>G , CM000673.1:g.4112770C>G	GRCh37
NC_000011.8:g.4069346C>G	NCBI36
NG_016277.1:g.240838C>G , LRG_164:g.240838C>G
NG_027992.2:g.1847C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*214C>G	ENSP00000432210.2:n.*214C>G
ENST00000698910.1:c.1311C>G	ENSP00000514024.1:p.Ser437Arg
ENST00000698911.1:c.1896C>G	ENSP00000514025.1:p.Ser632Arg
ENST00000698912.1:c.*214C>G	ENSP00000514026.1:n.*214C>G
ENST00000698913.1:c.1578C>G	ENSP00000514027.1:p.Ser526Arg
ENST00000698915.1:c.1884C>G	ENSP00000514029.1:p.Ser628Arg
ENST00000698916.1:c.1821C>G	ENSP00000514030.1:p.Ser607Arg
ENST00000698918.1:c.*1538C>G	ENSP00000514031.1:n.*1538C>G
ENST00000698919.1:c.*733C>G	ENSP00000514032.1:n.*733C>G
ENST00000698920.1:n.1100C>G
ENST00000526596.2:c.1893C>G MANE Select	ENSP00000433266.2:p.Ser631Arg
ENST00000300737.8:c.1800C>G	ENSP00000300737.4:p.Ser600Arg
ENST00000526156.1:n.598C>G
ENST00000526596.1:c.1085C>G
ENST00000527651.5:c.*214C>G	ENSP00000436208.1:n.*214C>G
ENST00000533977.5:c.1281C>G	ENSP00000434767.1:p.Ser427Arg
ENST00000616714.4:c.2118C>G	ENSP00000478059.1:p.Ser706Arg
NM_001277961.1:c.2118C>G	NP_001264890.1:p.Ser706Arg
NM_001277962.1:c.*214C>G	NP_001264891.1:n.*214C>G
NM_003156.3:c.1800C>G , LRG_164t1:c.1800C>G	NP_003147.2:p.Ser600Arg
NM_001277962.2:c.*214C>G	NP_001264891.1:n.*214C>G
NM_001277961.3:c.2118C>G	NP_001264890.1:p.Ser706Arg
NM_001382566.1:c.1896C>G	NP_001369495.1:p.Ser632Arg
NM_001382567.1:c.1893C>G MANE Select	NP_001369496.1:p.Ser631Arg
NM_001382568.1:c.1821C>G	NP_001369497.1:p.Ser607Arg
NM_001382569.1:c.1665C>G	NP_001369498.1:p.Ser555Arg
NM_001382570.1:c.1572C>G	NP_001369499.1:p.Ser524Arg
NM_001382571.1:c.1320C>G	NP_001369500.1:p.Ser440Arg
NM_001382575.1:c.1578C>G	NP_001369504.1:p.Ser526Arg
NM_001382576.1:c.1578C>G	NP_001369505.1:p.Ser526Arg
NM_001382577.1:c.1578C>G	NP_001369506.1:p.Ser526Arg
NM_001382578.1:c.*214C>G	NP_001369507.1:n.*214C>G
NM_001382579.1:c.*214C>G	NP_001369508.1:n.*214C>G
NM_001382580.1:c.*214C>G	NP_001369509.1:n.*214C>G
NM_001382581.1:c.1311C>G	NP_001369510.1:p.Ser437Arg
NM_003156.4:c.1800C>G	NP_003147.2:p.Ser600Arg
NR_168436.1:n.1724C>G
NR_168437.1:n.2229C>G
NR_168438.1:n.2051C>G