Canonical Allele Identifier: CA379194253

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4104594T>C (hg19) ; chr11:g.4083364T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083364T>C , CM000673.2:g.4083364T>C	GRCh38
NC_000011.9:g.4104594T>C , CM000673.1:g.4104594T>C	GRCh37
NC_000011.8:g.4061170T>C	NCBI36
NG_016277.1:g.232662T>C , LRG_164:g.232662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1118T>C	ENSP00000432210.2:p.Ile373Thr
ENST00000533343.2:n.1939T>C
ENST00000698909.1:n.2197T>C
ENST00000698910.1:c.851T>C	ENSP00000514024.1:p.Ile284Thr
ENST00000698911.1:c.1118T>C	ENSP00000514025.1:p.Ile373Thr
ENST00000698912.1:c.1118T>C	ENSP00000514026.1:p.Ile373Thr
ENST00000698913.1:c.1118T>C	ENSP00000514027.1:p.Ile373Thr
ENST00000698915.1:c.1340T>C	ENSP00000514029.1:p.Ile447Thr
ENST00000698916.1:c.1361T>C	ENSP00000514030.1:p.Ile454Thr
ENST00000698918.1:c.*1041T>C	ENSP00000514031.1:n.*1041T>C
ENST00000698919.1:c.*273T>C	ENSP00000514032.1:n.*273T>C
ENST00000698920.1:n.640T>C
ENST00000526596.2:c.1340T>C MANE Select	ENSP00000433266.2:p.Ile447Thr
ENST00000300737.8:c.1340T>C	ENSP00000300737.4:p.Ile447Thr
ENST00000526596.1:c.532T>C
ENST00000527651.5:c.1340T>C	ENSP00000436208.1:p.Ile447Thr
ENST00000531332.1:n.208T>C
ENST00000533343.1:n.350T>C
ENST00000533977.5:c.821T>C	ENSP00000434767.1:p.Ile274Thr
ENST00000616714.4:c.1340T>C	ENSP00000478059.1:p.Ile447Thr
NM_001277961.1:c.1340T>C	NP_001264890.1:p.Ile447Thr
NM_001277962.1:c.1340T>C	NP_001264891.1:p.Ile447Thr
NM_003156.3:c.1340T>C , LRG_164t1:c.1340T>C	NP_003147.2:p.Ile447Thr
NM_001277962.2:c.1340T>C	NP_001264891.1:p.Ile447Thr
NM_001277961.3:c.1340T>C	NP_001264890.1:p.Ile447Thr
NM_001382566.1:c.1118T>C	NP_001369495.1:p.Ile373Thr
NM_001382567.1:c.1340T>C MANE Select	NP_001369496.1:p.Ile447Thr
NM_001382568.1:c.1361T>C	NP_001369497.1:p.Ile454Thr
NM_001382569.1:c.1205T>C	NP_001369498.1:p.Ile402Thr
NM_001382570.1:c.1112T>C	NP_001369499.1:p.Ile371Thr
NM_001382571.1:c.860T>C	NP_001369500.1:p.Ile287Thr
NM_001382573.1:c.1118T>C	NP_001369502.1:p.Ile373Thr
NM_001382575.1:c.1118T>C	NP_001369504.1:p.Ile373Thr
NM_001382576.1:c.1118T>C	NP_001369505.1:p.Ile373Thr
NM_001382577.1:c.1118T>C	NP_001369506.1:p.Ile373Thr
NM_001382578.1:c.1118T>C	NP_001369507.1:p.Ile373Thr
NM_001382579.1:c.1118T>C	NP_001369508.1:p.Ile373Thr
NM_001382580.1:c.851T>C	NP_001369509.1:p.Ile284Thr
NM_001382581.1:c.851T>C	NP_001369510.1:p.Ile284Thr
NM_003156.4:c.1340T>C	NP_003147.2:p.Ile447Thr
NR_168436.1:n.1399-3113T>C
NR_168437.1:n.1769T>C
NR_168438.1:n.1591T>C