Canonical Allele Identifier: CA379197451
Gene: STIM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4091545C>A , CM000673.2:g.4091545C>A GRCh38
NC_000011.9:g.4112775C>A , CM000673.1:g.4112775C>A GRCh37
NC_000011.8:g.4069351C>A NCBI36
NG_016277.1:g.240843C>A , LRG_164:g.240843C>A
NG_027992.2:g.1852C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.*219C>A ENSP00000432210.2:n.*219C>A
ENST00000698910.1:c.1316C>A ENSP00000514024.1:p.Ser439Ter
ENST00000698911.1:c.1901C>A ENSP00000514025.1:p.Ser634Ter
ENST00000698912.1:c.*219C>A ENSP00000514026.1:n.*219C>A
ENST00000698913.1:c.1583C>A ENSP00000514027.1:p.Ser528Ter
ENST00000698915.1:c.1889C>A ENSP00000514029.1:p.Ser630Ter
ENST00000698916.1:c.1826C>A ENSP00000514030.1:p.Ser609Ter
ENST00000698918.1:c.*1543C>A ENSP00000514031.1:n.*1543C>A
ENST00000698919.1:c.*738C>A ENSP00000514032.1:n.*738C>A
ENST00000698920.1:n.1105C>A
ENST00000526596.2:c.1898C>A MANE Select ENSP00000433266.2:p.Ser633Ter
ENST00000300737.8:c.1805C>A ENSP00000300737.4:p.Ser602Ter
ENST00000526156.1:n.603C>A
ENST00000526596.1:c.1090C>A
ENST00000527651.5:c.*219C>A ENSP00000436208.1:n.*219C>A
ENST00000533977.5:c.1286C>A ENSP00000434767.1:p.Ser429Ter
ENST00000616714.4:c.2123C>A ENSP00000478059.1:p.Ser708Ter
NM_001277961.1:c.2123C>A NP_001264890.1:p.Ser708Ter
NM_001277962.1:c.*219C>A NP_001264891.1:n.*219C>A
NM_003156.3:c.1805C>A , LRG_164t1:c.1805C>A NP_003147.2:p.Ser602Ter
NM_001277962.2:c.*219C>A NP_001264891.1:n.*219C>A
NM_001277961.3:c.2123C>A NP_001264890.1:p.Ser708Ter
NM_001382566.1:c.1901C>A NP_001369495.1:p.Ser634Ter
NM_001382567.1:c.1898C>A MANE Select NP_001369496.1:p.Ser633Ter
NM_001382568.1:c.1826C>A NP_001369497.1:p.Ser609Ter
NM_001382569.1:c.1670C>A NP_001369498.1:p.Ser557Ter
NM_001382570.1:c.1577C>A NP_001369499.1:p.Ser526Ter
NM_001382571.1:c.1325C>A NP_001369500.1:p.Ser442Ter
NM_001382575.1:c.1583C>A NP_001369504.1:p.Ser528Ter
NM_001382576.1:c.1583C>A NP_001369505.1:p.Ser528Ter
NM_001382577.1:c.1583C>A NP_001369506.1:p.Ser528Ter
NM_001382578.1:c.*219C>A NP_001369507.1:n.*219C>A
NM_001382579.1:c.*219C>A NP_001369508.1:n.*219C>A
NM_001382580.1:c.*219C>A NP_001369509.1:n.*219C>A
NM_001382581.1:c.1316C>A NP_001369510.1:p.Ser439Ter
NM_003156.4:c.1805C>A NP_003147.2:p.Ser602Ter
NR_168436.1:n.1729C>A
NR_168437.1:n.2234C>A
NR_168438.1:n.2056C>A