Canonical Allele Identifier: CA2612107195

Gene: STIM1

Linked Data

• gnomAD v4: 11-4083130-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083130T>G , CM000673.2:g.4083130T>G	GRCh38
NC_000011.9:g.4104360T>G , CM000673.1:g.4104360T>G	GRCh37
NC_000011.8:g.4060936T>G	NCBI36
NG_016277.1:g.232428T>G , LRG_164:g.232428T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525403.6:c.1017-133T>G	ENSP00000432210.2:n.1017-133T>G
ENST00000533343.2:n.1838-133T>G
ENST00000698909.1:n.1963T>G
ENST00000698910.1:c.750-133T>G	ENSP00000514024.1:n.750-133T>G
ENST00000698911.1:c.1017-133T>G	ENSP00000514025.1:n.1017-133T>G
ENST00000698912.1:c.1017-133T>G	ENSP00000514026.1:n.1017-133T>G
ENST00000698913.1:c.1017-133T>G	ENSP00000514027.1:n.1017-133T>G
ENST00000698915.1:c.1239-133T>G	ENSP00000514029.1:n.1239-133T>G
ENST00000698916.1:c.1260-133T>G	ENSP00000514030.1:n.1260-133T>G
ENST00000698918.1:c.*940-133T>G	ENSP00000514031.1:n.*940-133T>G
ENST00000698919.1:c.*172-133T>G	ENSP00000514032.1:n.*172-133T>G
ENST00000698920.1:n.539-133T>G
ENST00000526596.2:c.1239-133T>G MANE Select	ENSP00000433266.2:n.1239-133T>G
ENST00000300737.8:c.1239-133T>G	ENSP00000300737.4:n.1239-133T>G
ENST00000526596.1:c.431-133T>G
ENST00000527651.5:c.1239-133T>G	ENSP00000436208.1:n.1239-133T>G
ENST00000533343.1:n.249-133T>G
ENST00000533977.5:c.720-133T>G	ENSP00000434767.1:n.720-133T>G
ENST00000616714.4:c.1239-133T>G	ENSP00000478059.1:n.1239-133T>G
NM_001277961.1:c.1239-133T>G	NP_001264890.1:n.1239-133T>G
NM_001277962.1:c.1239-133T>G	NP_001264891.1:n.1239-133T>G
NM_003156.3:c.1239-133T>G , LRG_164t1:c.1239-133T>G	NP_003147.2:n.1239-133T>G
NM_001277962.2:c.1239-133T>G	NP_001264891.1:n.1239-133T>G
NM_001277961.3:c.1239-133T>G	NP_001264890.1:n.1239-133T>G
NM_001382566.1:c.1017-133T>G	NP_001369495.1:n.1017-133T>G
NM_001382567.1:c.1239-133T>G MANE Select	NP_001369496.1:n.1239-133T>G
NM_001382568.1:c.1239-112T>G	NP_001369497.1:n.1239-112T>G
NM_001382569.1:c.1104-133T>G	NP_001369498.1:n.1104-133T>G
NM_001382570.1:c.1011-133T>G	NP_001369499.1:n.1011-133T>G
NM_001382571.1:c.759-133T>G	NP_001369500.1:n.759-133T>G
NM_001382573.1:c.1017-133T>G	NP_001369502.1:n.1017-133T>G
NM_001382575.1:c.1017-133T>G	NP_001369504.1:n.1017-133T>G
NM_001382576.1:c.1017-133T>G	NP_001369505.1:n.1017-133T>G
NM_001382577.1:c.1017-133T>G	NP_001369506.1:n.1017-133T>G
NM_001382578.1:c.1017-133T>G	NP_001369507.1:n.1017-133T>G
NM_001382579.1:c.1017-133T>G	NP_001369508.1:n.1017-133T>G
NM_001382580.1:c.750-133T>G	NP_001369509.1:n.750-133T>G
NM_001382581.1:c.750-133T>G	NP_001369510.1:n.750-133T>G
NM_003156.4:c.1239-133T>G	NP_003147.2:n.1239-133T>G
NR_168436.1:n.1399-3347T>G
NR_168437.1:n.1668-133T>G
NR_168438.1:n.1490-133T>G