Canonical Allele Identifier: CA1948976414
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4083406T= , CM000673.2:g.4083406T= GRCh38
NC_000011.9:g.4104636T= , CM000673.1:g.4104636T= GRCh37
NC_000011.8:g.4061212T= NCBI36
NG_016277.1:g.232704T= , LRG_164:g.232704T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.1160T= ENSP00000432210.2:p.Met387=
ENST00000533343.2:n.1981T=
ENST00000698909.1:n.2239T=
ENST00000698910.1:c.893T= ENSP00000514024.1:p.Met298=
ENST00000698911.1:c.1160T= ENSP00000514025.1:p.Met387=
ENST00000698912.1:c.1160T= ENSP00000514026.1:p.Met387=
ENST00000698913.1:c.1160T= ENSP00000514027.1:p.Met387=
ENST00000698915.1:c.1382T= ENSP00000514029.1:p.Met461=
ENST00000698916.1:c.1403T= ENSP00000514030.1:p.Met468=
ENST00000698918.1:c.*1083T= ENSP00000514031.1:n.*1083T=
ENST00000698919.1:c.*315T= ENSP00000514032.1:n.*315T=
ENST00000698920.1:n.682T=
ENST00000526596.2:c.1382T= MANE Select ENSP00000433266.2:p.Met461=
ENST00000300737.8:c.1382T= ENSP00000300737.4:p.Met461=
ENST00000526596.1:c.574T=
ENST00000527651.5:c.1382T= ENSP00000436208.1:p.Met461=
ENST00000531332.1:n.250T=
ENST00000533343.1:n.392T=
ENST00000533977.5:c.863T= ENSP00000434767.1:p.Met288=
ENST00000616714.4:c.1382T= ENSP00000478059.1:p.Met461=
NM_001277961.1:c.1382T= NP_001264890.1:p.Met461=
NM_001277962.1:c.1382T= NP_001264891.1:p.Met461=
NM_003156.3:c.1382T= , LRG_164t1:c.1382T= NP_003147.2:p.Met461=
NM_001277962.2:c.1382T= NP_001264891.1:p.Met461=
NM_001277961.3:c.1382T= NP_001264890.1:p.Met461=
NM_001382566.1:c.1160T= NP_001369495.1:p.Met387=
NM_001382567.1:c.1382T= MANE Select NP_001369496.1:p.Met461=
NM_001382568.1:c.1403T= NP_001369497.1:p.Met468=
NM_001382569.1:c.1247T= NP_001369498.1:p.Met416=
NM_001382570.1:c.1154T= NP_001369499.1:p.Met385=
NM_001382571.1:c.902T= NP_001369500.1:p.Met301=
NM_001382573.1:c.1160T= NP_001369502.1:p.Met387=
NM_001382575.1:c.1160T= NP_001369504.1:p.Met387=
NM_001382576.1:c.1160T= NP_001369505.1:p.Met387=
NM_001382577.1:c.1160T= NP_001369506.1:p.Met387=
NM_001382578.1:c.1160T= NP_001369507.1:p.Met387=
NM_001382579.1:c.1160T= NP_001369508.1:p.Met387=
NM_001382580.1:c.893T= NP_001369509.1:p.Met298=
NM_001382581.1:c.893T= NP_001369510.1:p.Met298=
NM_003156.4:c.1382T= NP_003147.2:p.Met461=
NR_168436.1:n.1399-3071T=
NR_168437.1:n.1811T=
NR_168438.1:n.1633T=