Canonical Allele Identifier: CA379197407

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112763A>T (hg19) ; chr11:g.4091533A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091533A>T , CM000673.2:g.4091533A>T	GRCh38
NC_000011.9:g.4112763A>T , CM000673.1:g.4112763A>T	GRCh37
NC_000011.8:g.4069339A>T	NCBI36
NG_016277.1:g.240831A>T , LRG_164:g.240831A>T
NG_027992.2:g.1840A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*207A>T	ENSP00000432210.2:n.*207A>T
ENST00000698910.1:c.1304A>T	ENSP00000514024.1:p.Glu435Val
ENST00000698911.1:c.1889A>T	ENSP00000514025.1:p.Glu630Val
ENST00000698912.1:c.*207A>T	ENSP00000514026.1:n.*207A>T
ENST00000698913.1:c.1571A>T	ENSP00000514027.1:p.Glu524Val
ENST00000698915.1:c.1877A>T	ENSP00000514029.1:p.Glu626Val
ENST00000698916.1:c.1814A>T	ENSP00000514030.1:p.Glu605Val
ENST00000698918.1:c.*1531A>T	ENSP00000514031.1:n.*1531A>T
ENST00000698919.1:c.*726A>T	ENSP00000514032.1:n.*726A>T
ENST00000698920.1:n.1093A>T
ENST00000526596.2:c.1886A>T MANE Select	ENSP00000433266.2:p.Glu629Val
ENST00000300737.8:c.1793A>T	ENSP00000300737.4:p.Glu598Val
ENST00000526156.1:n.591A>T
ENST00000526596.1:c.1078A>T
ENST00000527651.5:c.*207A>T	ENSP00000436208.1:n.*207A>T
ENST00000533977.5:c.1274A>T	ENSP00000434767.1:p.Glu425Val
ENST00000616714.4:c.2111A>T	ENSP00000478059.1:p.Glu704Val
NM_001277961.1:c.2111A>T	NP_001264890.1:p.Glu704Val
NM_001277962.1:c.*207A>T	NP_001264891.1:n.*207A>T
NM_003156.3:c.1793A>T , LRG_164t1:c.1793A>T	NP_003147.2:p.Glu598Val
NM_001277962.2:c.*207A>T	NP_001264891.1:n.*207A>T
NM_001277961.3:c.2111A>T	NP_001264890.1:p.Glu704Val
NM_001382566.1:c.1889A>T	NP_001369495.1:p.Glu630Val
NM_001382567.1:c.1886A>T MANE Select	NP_001369496.1:p.Glu629Val
NM_001382568.1:c.1814A>T	NP_001369497.1:p.Glu605Val
NM_001382569.1:c.1658A>T	NP_001369498.1:p.Glu553Val
NM_001382570.1:c.1565A>T	NP_001369499.1:p.Glu522Val
NM_001382571.1:c.1313A>T	NP_001369500.1:p.Glu438Val
NM_001382575.1:c.1571A>T	NP_001369504.1:p.Glu524Val
NM_001382576.1:c.1571A>T	NP_001369505.1:p.Glu524Val
NM_001382577.1:c.1571A>T	NP_001369506.1:p.Glu524Val
NM_001382578.1:c.*207A>T	NP_001369507.1:n.*207A>T
NM_001382579.1:c.*207A>T	NP_001369508.1:n.*207A>T
NM_001382580.1:c.*207A>T	NP_001369509.1:n.*207A>T
NM_001382581.1:c.1304A>T	NP_001369510.1:p.Glu435Val
NM_003156.4:c.1793A>T	NP_003147.2:p.Glu598Val
NR_168436.1:n.1717A>T
NR_168437.1:n.2222A>T
NR_168438.1:n.2044A>T