Canonical Allele Identifier: CA472869718

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112785T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091555T>A , CM000673.2:g.4091555T>A	GRCh38
NC_000011.9:g.4112785T>A , CM000673.1:g.4112785T>A	GRCh37
NC_000011.8:g.4069361T>A	NCBI36
NG_016277.1:g.240853T>A , LRG_164:g.240853T>A
NG_027992.2:g.1862T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*229T>A	ENSP00000432210.2:n.*229T>A
ENST00000698910.1:c.1326T>A	ENSP00000514024.1:p.Pro442=
ENST00000698911.1:c.1911T>A	ENSP00000514025.1:p.Pro637=
ENST00000698912.1:c.*229T>A	ENSP00000514026.1:n.*229T>A
ENST00000698913.1:c.1593T>A	ENSP00000514027.1:p.Pro531=
ENST00000698915.1:c.1899T>A	ENSP00000514029.1:p.Pro633=
ENST00000698916.1:c.1836T>A	ENSP00000514030.1:p.Pro612=
ENST00000698918.1:c.*1553T>A	ENSP00000514031.1:n.*1553T>A
ENST00000698919.1:c.*748T>A	ENSP00000514032.1:n.*748T>A
ENST00000698920.1:n.1115T>A
ENST00000526596.2:c.1908T>A MANE Select	ENSP00000433266.2:p.Pro636=
ENST00000300737.8:c.1815T>A	ENSP00000300737.4:p.Pro605=
ENST00000526156.1:n.613T>A
ENST00000526596.1:c.1100T>A
ENST00000527651.5:c.*229T>A	ENSP00000436208.1:n.*229T>A
ENST00000533977.5:c.1296T>A	ENSP00000434767.1:p.Pro432=
ENST00000616714.4:c.2133T>A	ENSP00000478059.1:p.Pro711=
NM_001277961.1:c.2133T>A	NP_001264890.1:p.Pro711=
NM_001277962.1:c.*229T>A	NP_001264891.1:n.*229T>A
NM_003156.3:c.1815T>A , LRG_164t1:c.1815T>A	NP_003147.2:p.Pro605=
NM_001277962.2:c.*229T>A	NP_001264891.1:n.*229T>A
NM_001277961.3:c.2133T>A	NP_001264890.1:p.Pro711=
NM_001382566.1:c.1911T>A	NP_001369495.1:p.Pro637=
NM_001382567.1:c.1908T>A MANE Select	NP_001369496.1:p.Pro636=
NM_001382568.1:c.1836T>A	NP_001369497.1:p.Pro612=
NM_001382569.1:c.1680T>A	NP_001369498.1:p.Pro560=
NM_001382570.1:c.1587T>A	NP_001369499.1:p.Pro529=
NM_001382571.1:c.1335T>A	NP_001369500.1:p.Pro445=
NM_001382575.1:c.1593T>A	NP_001369504.1:p.Pro531=
NM_001382576.1:c.1593T>A	NP_001369505.1:p.Pro531=
NM_001382577.1:c.1593T>A	NP_001369506.1:p.Pro531=
NM_001382578.1:c.*229T>A	NP_001369507.1:n.*229T>A
NM_001382579.1:c.*229T>A	NP_001369508.1:n.*229T>A
NM_001382580.1:c.*229T>A	NP_001369509.1:n.*229T>A
NM_001382581.1:c.1326T>A	NP_001369510.1:p.Pro442=
NM_003156.4:c.1815T>A	NP_003147.2:p.Pro605=
NR_168436.1:n.1739T>A
NR_168437.1:n.2244T>A
NR_168438.1:n.2066T>A