Canonical Allele Identifier: CA379197443

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112772C>G (hg19) ; chr11:g.4091542C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091542C>G , CM000673.2:g.4091542C>G	GRCh38
NC_000011.9:g.4112772C>G , CM000673.1:g.4112772C>G	GRCh37
NC_000011.8:g.4069348C>G	NCBI36
NG_016277.1:g.240840C>G , LRG_164:g.240840C>G
NG_027992.2:g.1849C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*216C>G	ENSP00000432210.2:n.*216C>G
ENST00000698910.1:c.1313C>G	ENSP00000514024.1:p.Pro438Arg
ENST00000698911.1:c.1898C>G	ENSP00000514025.1:p.Pro633Arg
ENST00000698912.1:c.*216C>G	ENSP00000514026.1:n.*216C>G
ENST00000698913.1:c.1580C>G	ENSP00000514027.1:p.Pro527Arg
ENST00000698915.1:c.1886C>G	ENSP00000514029.1:p.Pro629Arg
ENST00000698916.1:c.1823C>G	ENSP00000514030.1:p.Pro608Arg
ENST00000698918.1:c.*1540C>G	ENSP00000514031.1:n.*1540C>G
ENST00000698919.1:c.*735C>G	ENSP00000514032.1:n.*735C>G
ENST00000698920.1:n.1102C>G
ENST00000526596.2:c.1895C>G MANE Select	ENSP00000433266.2:p.Pro632Arg
ENST00000300737.8:c.1802C>G	ENSP00000300737.4:p.Pro601Arg
ENST00000526156.1:n.600C>G
ENST00000526596.1:c.1087C>G
ENST00000527651.5:c.*216C>G	ENSP00000436208.1:n.*216C>G
ENST00000533977.5:c.1283C>G	ENSP00000434767.1:p.Pro428Arg
ENST00000616714.4:c.2120C>G	ENSP00000478059.1:p.Pro707Arg
NM_001277961.1:c.2120C>G	NP_001264890.1:p.Pro707Arg
NM_001277962.1:c.*216C>G	NP_001264891.1:n.*216C>G
NM_003156.3:c.1802C>G , LRG_164t1:c.1802C>G	NP_003147.2:p.Pro601Arg
NM_001277962.2:c.*216C>G	NP_001264891.1:n.*216C>G
NM_001277961.3:c.2120C>G	NP_001264890.1:p.Pro707Arg
NM_001382566.1:c.1898C>G	NP_001369495.1:p.Pro633Arg
NM_001382567.1:c.1895C>G MANE Select	NP_001369496.1:p.Pro632Arg
NM_001382568.1:c.1823C>G	NP_001369497.1:p.Pro608Arg
NM_001382569.1:c.1667C>G	NP_001369498.1:p.Pro556Arg
NM_001382570.1:c.1574C>G	NP_001369499.1:p.Pro525Arg
NM_001382571.1:c.1322C>G	NP_001369500.1:p.Pro441Arg
NM_001382575.1:c.1580C>G	NP_001369504.1:p.Pro527Arg
NM_001382576.1:c.1580C>G	NP_001369505.1:p.Pro527Arg
NM_001382577.1:c.1580C>G	NP_001369506.1:p.Pro527Arg
NM_001382578.1:c.*216C>G	NP_001369507.1:n.*216C>G
NM_001382579.1:c.*216C>G	NP_001369508.1:n.*216C>G
NM_001382580.1:c.*216C>G	NP_001369509.1:n.*216C>G
NM_001382581.1:c.1313C>G	NP_001369510.1:p.Pro438Arg
NM_003156.4:c.1802C>G	NP_003147.2:p.Pro601Arg
NR_168436.1:n.1726C>G
NR_168437.1:n.2231C>G
NR_168438.1:n.2053C>G