Canonical Allele Identifier: CA379485081

Gene: STIM1

Linked Data

• COSMIC: COSM224387
• MyVariant Identifiers: chr11:g.3988890T>C (hg19) ; chr11:g.3967660T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.3967660T>C , CM000673.2:g.3967660T>C	GRCh38
NC_000011.9:g.3988890T>C , CM000673.1:g.3988890T>C	GRCh37
NC_000011.8:g.3945466T>C	NCBI36
NG_016277.1:g.116958T>C , LRG_164:g.116958T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.26T>C	ENSP00000432210.2:p.Val9Ala
ENST00000533343.2:n.847T>C
ENST00000698909.1:n.295T>C
ENST00000698910.1:c.-219-56213T>C	ENSP00000514024.1:n.-219-56213T>C
ENST00000698911.1:c.26T>C	ENSP00000514025.1:p.Val9Ala
ENST00000698912.1:c.26T>C	ENSP00000514026.1:p.Val9Ala
ENST00000698913.1:c.26T>C	ENSP00000514027.1:p.Val9Ala
ENST00000698914.1:c.248T>C	ENSP00000514028.1:p.Val83Ala
ENST00000698915.1:c.248T>C	ENSP00000514029.1:p.Val83Ala
ENST00000698916.1:c.248T>C	ENSP00000514030.1:p.Val83Ala
ENST00000698917.1:n.487T>C
ENST00000698918.1:c.140-56213T>C	ENSP00000514031.1:n.140-56213T>C
ENST00000698919.1:c.248T>C	ENSP00000514032.1:p.Val83Ala
ENST00000526596.2:c.248T>C MANE Select	ENSP00000433266.2:p.Val83Ala
ENST00000300737.8:c.248T>C	ENSP00000300737.4:p.Val83Ala
ENST00000524822.5:c.26T>C	ENSP00000434200.1:p.Val9Ala
ENST00000525055.5:c.26T>C	ENSP00000431191.1:p.Val9Ala
ENST00000525403.5:c.26T>C	ENSP00000432210.1:p.Val9Ala
ENST00000527651.5:c.248T>C	ENSP00000436208.1:p.Val83Ala
ENST00000528656.5:c.26T>C	ENSP00000432378.1:p.Val9Ala
ENST00000530554.5:c.26T>C	ENSP00000431878.1:p.Val9Ala
ENST00000532610.5:c.26T>C	ENSP00000434848.1:p.Val9Ala
ENST00000532919.5:c.26T>C	ENSP00000433949.1:p.Val9Ala
ENST00000532990.1:c.26T>C	ENSP00000432383.1:p.Val9Ala
ENST00000616714.4:c.248T>C	ENSP00000478059.1:p.Val83Ala
NM_001277961.1:c.248T>C	NP_001264890.1:p.Val83Ala
NM_001277962.1:c.248T>C	NP_001264891.1:p.Val83Ala
NM_003156.3:c.248T>C , LRG_164t1:c.248T>C	NP_003147.2:p.Val83Ala
NM_001277962.2:c.248T>C	NP_001264891.1:p.Val83Ala
NM_001277961.3:c.248T>C	NP_001264890.1:p.Val83Ala
NM_001382566.1:c.26T>C	NP_001369495.1:p.Val9Ala
NM_001382567.1:c.248T>C MANE Select	NP_001369496.1:p.Val83Ala
NM_001382568.1:c.248T>C	NP_001369497.1:p.Val83Ala
NM_001382569.1:c.136-56213T>C	NP_001369498.1:n.136-56213T>C
NM_001382570.1:c.248T>C	NP_001369499.1:p.Val83Ala
NM_001382571.1:c.-98-56213T>C	NP_001369500.1:n.-98-56213T>C
NM_001382572.1:c.248T>C	NP_001369501.1:p.Val83Ala
NM_001382573.1:c.26T>C	NP_001369502.1:p.Val9Ala
NM_001382574.1:c.26T>C	NP_001369503.1:p.Val9Ala
NM_001382575.1:c.26T>C	NP_001369504.1:p.Val9Ala
NM_001382576.1:c.26T>C	NP_001369505.1:p.Val9Ala
NM_001382577.1:c.26T>C	NP_001369506.1:p.Val9Ala
NM_001382578.1:c.26T>C	NP_001369507.1:p.Val9Ala
NM_001382579.1:c.26T>C	NP_001369508.1:p.Val9Ala
NM_001382580.1:c.-219-56213T>C	NP_001369509.1:n.-219-56213T>C
NM_001382581.1:c.-219-56213T>C	NP_001369510.1:n.-219-56213T>C
NM_003156.4:c.248T>C	NP_003147.2:p.Val83Ala
NR_168436.1:n.855T>C
NR_168437.1:n.855T>C
NR_168438.1:n.855T>C