Canonical Allele Identifier: CA2790247704

Gene: STIM1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4083550G>A , CM000673.2:g.4083550G>A	GRCh38
NC_000011.9:g.4104780G>A , CM000673.1:g.4104780G>A	GRCh37
NC_000011.8:g.4061356G>A	NCBI36
NG_016277.1:g.232848G>A , LRG_164:g.232848G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.1252+52G>A	ENSP00000432210.2:n.1252+52G>A
ENST00000533343.2:n.2125G>A
ENST00000698909.1:n.2331+52G>A
ENST00000698910.1:c.985+52G>A	ENSP00000514024.1:n.985+52G>A
ENST00000698911.1:c.1252+52G>A	ENSP00000514025.1:n.1252+52G>A
ENST00000698912.1:c.1252+52G>A	ENSP00000514026.1:n.1252+52G>A
ENST00000698913.1:c.1252+52G>A	ENSP00000514027.1:n.1252+52G>A
ENST00000698915.1:c.1474+52G>A	ENSP00000514029.1:n.1474+52G>A
ENST00000698916.1:c.1495+52G>A	ENSP00000514030.1:n.1495+52G>A
ENST00000698918.1:c.*1175+52G>A	ENSP00000514031.1:n.*1175+52G>A
ENST00000698919.1:c.*407+52G>A	ENSP00000514032.1:n.*407+52G>A
ENST00000698920.1:n.774+52G>A
ENST00000526596.2:c.1474+52G>A MANE Select	ENSP00000433266.2:n.1474+52G>A
ENST00000300737.8:c.1474+52G>A	ENSP00000300737.4:n.1474+52G>A
ENST00000526596.1:c.666+52G>A
ENST00000527651.5:c.1474+52G>A	ENSP00000436208.1:n.1474+52G>A
ENST00000531332.1:n.342+52G>A
ENST00000533343.1:n.536G>A
ENST00000533977.5:c.955+52G>A	ENSP00000434767.1:n.955+52G>A
ENST00000616714.4:c.1474+52G>A	ENSP00000478059.1:n.1474+52G>A
NM_001277961.1:c.1474+52G>A	NP_001264890.1:n.1474+52G>A
NM_001277962.1:c.1474+52G>A	NP_001264891.1:n.1474+52G>A
NM_003156.3:c.1474+52G>A , LRG_164t1:c.1474+52G>A	NP_003147.2:n.1474+52G>A
NM_001277962.2:c.1474+52G>A	NP_001264891.1:n.1474+52G>A
NM_001277961.3:c.1474+52G>A	NP_001264890.1:n.1474+52G>A
NM_001382566.1:c.1252+52G>A	NP_001369495.1:n.1252+52G>A
NM_001382567.1:c.1474+52G>A MANE Select	NP_001369496.1:n.1474+52G>A
NM_001382568.1:c.1495+52G>A	NP_001369497.1:n.1495+52G>A
NM_001382569.1:c.1339+52G>A	NP_001369498.1:n.1339+52G>A
NM_001382570.1:c.1246+52G>A	NP_001369499.1:n.1246+52G>A
NM_001382571.1:c.994+52G>A	NP_001369500.1:n.994+52G>A
NM_001382573.1:c.*44G>A	NP_001369502.1:n.*44G>A
NM_001382575.1:c.1252+52G>A	NP_001369504.1:n.1252+52G>A
NM_001382576.1:c.1252+52G>A	NP_001369505.1:n.1252+52G>A
NM_001382577.1:c.1252+52G>A	NP_001369506.1:n.1252+52G>A
NM_001382578.1:c.1252+52G>A	NP_001369507.1:n.1252+52G>A
NM_001382579.1:c.1252+52G>A	NP_001369508.1:n.1252+52G>A
NM_001382580.1:c.985+52G>A	NP_001369509.1:n.985+52G>A
NM_001382581.1:c.985+52G>A	NP_001369510.1:n.985+52G>A
NM_003156.4:c.1474+52G>A	NP_003147.2:n.1474+52G>A
NR_168436.1:n.1399-2927G>A
NR_168437.1:n.1903+52G>A
NR_168438.1:n.1725+52G>A