Canonical Allele Identifier: CA2790247893
Gene: STIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4091539_4091540insTT , CM000673.2:g.4091539_4091540insTT GRCh38
NC_000011.9:g.4112769_4112770insTT , CM000673.1:g.4112769_4112770insTT GRCh37
NC_000011.8:g.4069345_4069346insTT NCBI36
NG_016277.1:g.240837_240838insTT , LRG_164:g.240837_240838insTT
NG_027992.2:g.1846_1847insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.*213_*214insTT ENSP00000432210.2:n.*213_*214insTT
ENST00000698910.1:c.1310_1311insTT ENSP00000514024.1:p.Pro438SerfsTer?
ENST00000698911.1:c.1895_1896insTT ENSP00000514025.1:p.Pro633SerfsTer?
ENST00000698912.1:c.*213_*214insTT ENSP00000514026.1:n.*213_*214insTT
ENST00000698913.1:c.1577_1578insTT ENSP00000514027.1:p.Pro527SerfsTer?
ENST00000698915.1:c.1883_1884insTT ENSP00000514029.1:p.Pro629SerfsTer?
ENST00000698916.1:c.1820_1821insTT ENSP00000514030.1:p.Pro608SerfsTer?
ENST00000698918.1:c.*1537_*1538insTT ENSP00000514031.1:n.*1537_*1538insTT
ENST00000698919.1:c.*732_*733insTT ENSP00000514032.1:n.*732_*733insTT
ENST00000698920.1:n.1099_1100insTT
ENST00000526596.2:c.1892_1893insTT MANE Select ENSP00000433266.2:p.Pro632SerfsTer?
ENST00000300737.8:c.1799_1800insTT ENSP00000300737.4:p.Pro601SerfsTer?
ENST00000526156.1:n.597_598insTT
ENST00000526596.1:c.1084_1085insTT
ENST00000527651.5:c.*213_*214insTT ENSP00000436208.1:n.*213_*214insTT
ENST00000533977.5:c.1280_1281insTT ENSP00000434767.1:p.Pro428SerfsTer?
ENST00000616714.4:c.2117_2118insTT ENSP00000478059.1:p.Pro707SerfsTer?
NM_001277961.1:c.2117_2118insTT NP_001264890.1:p.Pro707SerfsTer?
NM_001277962.1:c.*213_*214insTT NP_001264891.1:n.*213_*214insTT
NM_003156.3:c.1799_1800insTT , LRG_164t1:c.1799_1800insTT NP_003147.2:p.Pro601SerfsTer?
NM_001277962.2:c.*213_*214insTT NP_001264891.1:n.*213_*214insTT
NM_001277961.3:c.2117_2118insTT NP_001264890.1:p.Pro707SerfsTer?
NM_001382566.1:c.1895_1896insTT NP_001369495.1:p.Pro633SerfsTer?
NM_001382567.1:c.1892_1893insTT MANE Select NP_001369496.1:p.Pro632SerfsTer?
NM_001382568.1:c.1820_1821insTT NP_001369497.1:p.Pro608SerfsTer?
NM_001382569.1:c.1664_1665insTT NP_001369498.1:p.Pro556SerfsTer?
NM_001382570.1:c.1571_1572insTT NP_001369499.1:p.Pro525SerfsTer?
NM_001382571.1:c.1319_1320insTT NP_001369500.1:p.Pro441SerfsTer?
NM_001382575.1:c.1577_1578insTT NP_001369504.1:p.Pro527SerfsTer?
NM_001382576.1:c.1577_1578insTT NP_001369505.1:p.Pro527SerfsTer?
NM_001382577.1:c.1577_1578insTT NP_001369506.1:p.Pro527SerfsTer?
NM_001382578.1:c.*213_*214insTT NP_001369507.1:n.*213_*214insTT
NM_001382579.1:c.*213_*214insTT NP_001369508.1:n.*213_*214insTT
NM_001382580.1:c.*213_*214insTT NP_001369509.1:n.*213_*214insTT
NM_001382581.1:c.1310_1311insTT NP_001369510.1:p.Pro438SerfsTer?
NM_003156.4:c.1799_1800insTT NP_003147.2:p.Pro601SerfsTer?
NR_168436.1:n.1723_1724insTT
NR_168437.1:n.2228_2229insTT
NR_168438.1:n.2050_2051insTT