Canonical Allele Identifier: CA472869261

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4104526G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083296G>C , CM000673.2:g.4083296G>C	GRCh38
NC_000011.9:g.4104526G>C , CM000673.1:g.4104526G>C	GRCh37
NC_000011.8:g.4061102G>C	NCBI36
NG_016277.1:g.232594G>C , LRG_164:g.232594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1050G>C	ENSP00000432210.2:p.Arg350=
ENST00000533343.2:n.1871G>C
ENST00000698909.1:n.2129G>C
ENST00000698910.1:c.783G>C	ENSP00000514024.1:p.Arg261=
ENST00000698911.1:c.1050G>C	ENSP00000514025.1:p.Arg350=
ENST00000698912.1:c.1050G>C	ENSP00000514026.1:p.Arg350=
ENST00000698913.1:c.1050G>C	ENSP00000514027.1:p.Arg350=
ENST00000698915.1:c.1272G>C	ENSP00000514029.1:p.Arg424=
ENST00000698916.1:c.1293G>C	ENSP00000514030.1:p.Arg431=
ENST00000698918.1:c.*973G>C	ENSP00000514031.1:n.*973G>C
ENST00000698919.1:c.*205G>C	ENSP00000514032.1:n.*205G>C
ENST00000698920.1:n.572G>C
ENST00000526596.2:c.1272G>C MANE Select	ENSP00000433266.2:p.Arg424=
ENST00000300737.8:c.1272G>C	ENSP00000300737.4:p.Arg424=
ENST00000526596.1:c.464G>C
ENST00000527651.5:c.1272G>C	ENSP00000436208.1:p.Arg424=
ENST00000531332.1:n.140G>C
ENST00000533343.1:n.282G>C
ENST00000533977.5:c.753G>C	ENSP00000434767.1:p.Arg251=
ENST00000616714.4:c.1272G>C	ENSP00000478059.1:p.Arg424=
NM_001277961.1:c.1272G>C	NP_001264890.1:p.Arg424=
NM_001277962.1:c.1272G>C	NP_001264891.1:p.Arg424=
NM_003156.3:c.1272G>C , LRG_164t1:c.1272G>C	NP_003147.2:p.Arg424=
NM_001277962.2:c.1272G>C	NP_001264891.1:p.Arg424=
NM_001277961.3:c.1272G>C	NP_001264890.1:p.Arg424=
NM_001382566.1:c.1050G>C	NP_001369495.1:p.Arg350=
NM_001382567.1:c.1272G>C MANE Select	NP_001369496.1:p.Arg424=
NM_001382568.1:c.1293G>C	NP_001369497.1:p.Arg431=
NM_001382569.1:c.1137G>C	NP_001369498.1:p.Arg379=
NM_001382570.1:c.1044G>C	NP_001369499.1:p.Arg348=
NM_001382571.1:c.792G>C	NP_001369500.1:p.Arg264=
NM_001382573.1:c.1050G>C	NP_001369502.1:p.Arg350=
NM_001382575.1:c.1050G>C	NP_001369504.1:p.Arg350=
NM_001382576.1:c.1050G>C	NP_001369505.1:p.Arg350=
NM_001382577.1:c.1050G>C	NP_001369506.1:p.Arg350=
NM_001382578.1:c.1050G>C	NP_001369507.1:p.Arg350=
NM_001382579.1:c.1050G>C	NP_001369508.1:p.Arg350=
NM_001382580.1:c.783G>C	NP_001369509.1:p.Arg261=
NM_001382581.1:c.783G>C	NP_001369510.1:p.Arg261=
NM_003156.4:c.1272G>C	NP_003147.2:p.Arg424=
NR_168436.1:n.1399-3181G>C
NR_168437.1:n.1701G>C
NR_168438.1:n.1523G>C