Canonical Allele Identifier: CA472869723

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112788T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091558T>A , CM000673.2:g.4091558T>A	GRCh38
NC_000011.9:g.4112788T>A , CM000673.1:g.4112788T>A	GRCh37
NC_000011.8:g.4069364T>A	NCBI36
NG_016277.1:g.240856T>A , LRG_164:g.240856T>A
NG_027992.2:g.1865T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*232T>A	ENSP00000432210.2:n.*232T>A
ENST00000698910.1:c.1329T>A	ENSP00000514024.1:p.Gly443=
ENST00000698911.1:c.1914T>A	ENSP00000514025.1:p.Gly638=
ENST00000698912.1:c.*232T>A	ENSP00000514026.1:n.*232T>A
ENST00000698913.1:c.1596T>A	ENSP00000514027.1:p.Gly532=
ENST00000698915.1:c.1902T>A	ENSP00000514029.1:p.Gly634=
ENST00000698916.1:c.1839T>A	ENSP00000514030.1:p.Gly613=
ENST00000698918.1:c.*1556T>A	ENSP00000514031.1:n.*1556T>A
ENST00000698919.1:c.*751T>A	ENSP00000514032.1:n.*751T>A
ENST00000698920.1:n.1118T>A
ENST00000526596.2:c.1911T>A MANE Select	ENSP00000433266.2:p.Gly637=
ENST00000300737.8:c.1818T>A	ENSP00000300737.4:p.Gly606=
ENST00000526156.1:n.616T>A
ENST00000526596.1:c.1103T>A
ENST00000527651.5:c.*232T>A	ENSP00000436208.1:n.*232T>A
ENST00000533977.5:c.1299T>A	ENSP00000434767.1:p.Gly433=
ENST00000616714.4:c.2136T>A	ENSP00000478059.1:p.Gly712=
NM_001277961.1:c.2136T>A	NP_001264890.1:p.Gly712=
NM_001277962.1:c.*232T>A	NP_001264891.1:n.*232T>A
NM_003156.3:c.1818T>A , LRG_164t1:c.1818T>A	NP_003147.2:p.Gly606=
NM_001277962.2:c.*232T>A	NP_001264891.1:n.*232T>A
NM_001277961.3:c.2136T>A	NP_001264890.1:p.Gly712=
NM_001382566.1:c.1914T>A	NP_001369495.1:p.Gly638=
NM_001382567.1:c.1911T>A MANE Select	NP_001369496.1:p.Gly637=
NM_001382568.1:c.1839T>A	NP_001369497.1:p.Gly613=
NM_001382569.1:c.1683T>A	NP_001369498.1:p.Gly561=
NM_001382570.1:c.1590T>A	NP_001369499.1:p.Gly530=
NM_001382571.1:c.1338T>A	NP_001369500.1:p.Gly446=
NM_001382575.1:c.1596T>A	NP_001369504.1:p.Gly532=
NM_001382576.1:c.1596T>A	NP_001369505.1:p.Gly532=
NM_001382577.1:c.1596T>A	NP_001369506.1:p.Gly532=
NM_001382578.1:c.*232T>A	NP_001369507.1:n.*232T>A
NM_001382579.1:c.*232T>A	NP_001369508.1:n.*232T>A
NM_001382580.1:c.*232T>A	NP_001369509.1:n.*232T>A
NM_001382581.1:c.1329T>A	NP_001369510.1:p.Gly443=
NM_003156.4:c.1818T>A	NP_003147.2:p.Gly606=
NR_168436.1:n.1742T>A
NR_168437.1:n.2247T>A
NR_168438.1:n.2069T>A