Canonical Allele Identifier: CA379197344

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112747G>A (hg19) ; chr11:g.4091517G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091517G>A , CM000673.2:g.4091517G>A	GRCh38
NC_000011.9:g.4112747G>A , CM000673.1:g.4112747G>A	GRCh37
NC_000011.8:g.4069323G>A	NCBI36
NG_016277.1:g.240815G>A , LRG_164:g.240815G>A
NG_027992.2:g.1824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*191G>A	ENSP00000432210.2:n.*191G>A
ENST00000698910.1:c.1288G>A	ENSP00000514024.1:p.Ala430Thr
ENST00000698911.1:c.1873G>A	ENSP00000514025.1:p.Ala625Thr
ENST00000698912.1:c.*191G>A	ENSP00000514026.1:n.*191G>A
ENST00000698913.1:c.1555G>A	ENSP00000514027.1:p.Ala519Thr
ENST00000698915.1:c.1861G>A	ENSP00000514029.1:p.Ala621Thr
ENST00000698916.1:c.1798G>A	ENSP00000514030.1:p.Ala600Thr
ENST00000698918.1:c.*1515G>A	ENSP00000514031.1:n.*1515G>A
ENST00000698919.1:c.*710G>A	ENSP00000514032.1:n.*710G>A
ENST00000698920.1:n.1077G>A
ENST00000526596.2:c.1870G>A MANE Select	ENSP00000433266.2:p.Ala624Thr
ENST00000300737.8:c.1777G>A	ENSP00000300737.4:p.Ala593Thr
ENST00000526156.1:n.575G>A
ENST00000526596.1:c.1062G>A
ENST00000527651.5:c.*191G>A	ENSP00000436208.1:n.*191G>A
ENST00000533977.5:c.1258G>A	ENSP00000434767.1:p.Ala420Thr
ENST00000616714.4:c.2095G>A	ENSP00000478059.1:p.Ala699Thr
NM_001277961.1:c.2095G>A	NP_001264890.1:p.Ala699Thr
NM_001277962.1:c.*191G>A	NP_001264891.1:n.*191G>A
NM_003156.3:c.1777G>A , LRG_164t1:c.1777G>A	NP_003147.2:p.Ala593Thr
NM_001277962.2:c.*191G>A	NP_001264891.1:n.*191G>A
NM_001277961.3:c.2095G>A	NP_001264890.1:p.Ala699Thr
NM_001382566.1:c.1873G>A	NP_001369495.1:p.Ala625Thr
NM_001382567.1:c.1870G>A MANE Select	NP_001369496.1:p.Ala624Thr
NM_001382568.1:c.1798G>A	NP_001369497.1:p.Ala600Thr
NM_001382569.1:c.1642G>A	NP_001369498.1:p.Ala548Thr
NM_001382570.1:c.1549G>A	NP_001369499.1:p.Ala517Thr
NM_001382571.1:c.1297G>A	NP_001369500.1:p.Ala433Thr
NM_001382575.1:c.1555G>A	NP_001369504.1:p.Ala519Thr
NM_001382576.1:c.1555G>A	NP_001369505.1:p.Ala519Thr
NM_001382577.1:c.1555G>A	NP_001369506.1:p.Ala519Thr
NM_001382578.1:c.*191G>A	NP_001369507.1:n.*191G>A
NM_001382579.1:c.*191G>A	NP_001369508.1:n.*191G>A
NM_001382580.1:c.*191G>A	NP_001369509.1:n.*191G>A
NM_001382581.1:c.1288G>A	NP_001369510.1:p.Ala430Thr
NM_003156.4:c.1777G>A	NP_003147.2:p.Ala593Thr
NR_168436.1:n.1701G>A
NR_168437.1:n.2206G>A
NR_168438.1:n.2028G>A