Canonical Allele Identifier: CA379197300

Gene: STIM1

Linked Data

• ClinVar Variation Id: 1010176
• ClinVar RCV Id: RCV001307765
• dbSNP Id: rs2094525006
• MyVariant Identifiers: chr11:g.4112736G>C (hg19) ; chr11:g.4091506G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091506G>C , CM000673.2:g.4091506G>C	GRCh38
NC_000011.9:g.4112736G>C , CM000673.1:g.4112736G>C	GRCh37
NC_000011.8:g.4069312G>C	NCBI36
NG_016277.1:g.240804G>C , LRG_164:g.240804G>C
NG_027992.2:g.1813G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*180G>C	ENSP00000432210.2:n.*180G>C
ENST00000698910.1:c.1277G>C	ENSP00000514024.1:p.Gly426Ala
ENST00000698911.1:c.1862G>C	ENSP00000514025.1:p.Gly621Ala
ENST00000698912.1:c.*180G>C	ENSP00000514026.1:n.*180G>C
ENST00000698913.1:c.1544G>C	ENSP00000514027.1:p.Gly515Ala
ENST00000698915.1:c.1850G>C	ENSP00000514029.1:p.Gly617Ala
ENST00000698916.1:c.1787G>C	ENSP00000514030.1:p.Gly596Ala
ENST00000698918.1:c.*1504G>C	ENSP00000514031.1:n.*1504G>C
ENST00000698919.1:c.*699G>C	ENSP00000514032.1:n.*699G>C
ENST00000698920.1:n.1066G>C
ENST00000526596.2:c.1859G>C MANE Select	ENSP00000433266.2:p.Gly620Ala
ENST00000300737.8:c.1766G>C	ENSP00000300737.4:p.Gly589Ala
ENST00000526156.1:n.564G>C
ENST00000526596.1:c.1051G>C
ENST00000527651.5:c.*180G>C	ENSP00000436208.1:n.*180G>C
ENST00000533977.5:c.1247G>C	ENSP00000434767.1:p.Gly416Ala
ENST00000616714.4:c.2084G>C	ENSP00000478059.1:p.Gly695Ala
NM_001277961.1:c.2084G>C	NP_001264890.1:p.Gly695Ala
NM_001277962.1:c.*180G>C	NP_001264891.1:n.*180G>C
NM_003156.3:c.1766G>C , LRG_164t1:c.1766G>C	NP_003147.2:p.Gly589Ala
NM_001277962.2:c.*180G>C	NP_001264891.1:n.*180G>C
NM_001277961.3:c.2084G>C	NP_001264890.1:p.Gly695Ala
NM_001382566.1:c.1862G>C	NP_001369495.1:p.Gly621Ala
NM_001382567.1:c.1859G>C MANE Select	NP_001369496.1:p.Gly620Ala
NM_001382568.1:c.1787G>C	NP_001369497.1:p.Gly596Ala
NM_001382569.1:c.1631G>C	NP_001369498.1:p.Gly544Ala
NM_001382570.1:c.1538G>C	NP_001369499.1:p.Gly513Ala
NM_001382571.1:c.1286G>C	NP_001369500.1:p.Gly429Ala
NM_001382575.1:c.1544G>C	NP_001369504.1:p.Gly515Ala
NM_001382576.1:c.1544G>C	NP_001369505.1:p.Gly515Ala
NM_001382577.1:c.1544G>C	NP_001369506.1:p.Gly515Ala
NM_001382578.1:c.*180G>C	NP_001369507.1:n.*180G>C
NM_001382579.1:c.*180G>C	NP_001369508.1:n.*180G>C
NM_001382580.1:c.*180G>C	NP_001369509.1:n.*180G>C
NM_001382581.1:c.1277G>C	NP_001369510.1:p.Gly426Ala
NM_003156.4:c.1766G>C	NP_003147.2:p.Gly589Ala
NR_168436.1:n.1690G>C
NR_168437.1:n.2195G>C
NR_168438.1:n.2017G>C