Canonical Allele Identifier: CA379197441

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112771C>G (hg19) ; chr11:g.4091541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091541C>G , CM000673.2:g.4091541C>G	GRCh38
NC_000011.9:g.4112771C>G , CM000673.1:g.4112771C>G	GRCh37
NC_000011.8:g.4069347C>G	NCBI36
NG_016277.1:g.240839C>G , LRG_164:g.240839C>G
NG_027992.2:g.1848C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*215C>G	ENSP00000432210.2:n.*215C>G
ENST00000698910.1:c.1312C>G	ENSP00000514024.1:p.Pro438Ala
ENST00000698911.1:c.1897C>G	ENSP00000514025.1:p.Pro633Ala
ENST00000698912.1:c.*215C>G	ENSP00000514026.1:n.*215C>G
ENST00000698913.1:c.1579C>G	ENSP00000514027.1:p.Pro527Ala
ENST00000698915.1:c.1885C>G	ENSP00000514029.1:p.Pro629Ala
ENST00000698916.1:c.1822C>G	ENSP00000514030.1:p.Pro608Ala
ENST00000698918.1:c.*1539C>G	ENSP00000514031.1:n.*1539C>G
ENST00000698919.1:c.*734C>G	ENSP00000514032.1:n.*734C>G
ENST00000698920.1:n.1101C>G
ENST00000526596.2:c.1894C>G MANE Select	ENSP00000433266.2:p.Pro632Ala
ENST00000300737.8:c.1801C>G	ENSP00000300737.4:p.Pro601Ala
ENST00000526156.1:n.599C>G
ENST00000526596.1:c.1086C>G
ENST00000527651.5:c.*215C>G	ENSP00000436208.1:n.*215C>G
ENST00000533977.5:c.1282C>G	ENSP00000434767.1:p.Pro428Ala
ENST00000616714.4:c.2119C>G	ENSP00000478059.1:p.Pro707Ala
NM_001277961.1:c.2119C>G	NP_001264890.1:p.Pro707Ala
NM_001277962.1:c.*215C>G	NP_001264891.1:n.*215C>G
NM_003156.3:c.1801C>G , LRG_164t1:c.1801C>G	NP_003147.2:p.Pro601Ala
NM_001277962.2:c.*215C>G	NP_001264891.1:n.*215C>G
NM_001277961.3:c.2119C>G	NP_001264890.1:p.Pro707Ala
NM_001382566.1:c.1897C>G	NP_001369495.1:p.Pro633Ala
NM_001382567.1:c.1894C>G MANE Select	NP_001369496.1:p.Pro632Ala
NM_001382568.1:c.1822C>G	NP_001369497.1:p.Pro608Ala
NM_001382569.1:c.1666C>G	NP_001369498.1:p.Pro556Ala
NM_001382570.1:c.1573C>G	NP_001369499.1:p.Pro525Ala
NM_001382571.1:c.1321C>G	NP_001369500.1:p.Pro441Ala
NM_001382575.1:c.1579C>G	NP_001369504.1:p.Pro527Ala
NM_001382576.1:c.1579C>G	NP_001369505.1:p.Pro527Ala
NM_001382577.1:c.1579C>G	NP_001369506.1:p.Pro527Ala
NM_001382578.1:c.*215C>G	NP_001369507.1:n.*215C>G
NM_001382579.1:c.*215C>G	NP_001369508.1:n.*215C>G
NM_001382580.1:c.*215C>G	NP_001369509.1:n.*215C>G
NM_001382581.1:c.1312C>G	NP_001369510.1:p.Pro438Ala
NM_003156.4:c.1801C>G	NP_003147.2:p.Pro601Ala
NR_168436.1:n.1725C>G
NR_168437.1:n.2230C>G
NR_168438.1:n.2052C>G