Canonical Allele Identifier: CA472869693

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112743C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091513C>T , CM000673.2:g.4091513C>T	GRCh38
NC_000011.9:g.4112743C>T , CM000673.1:g.4112743C>T	GRCh37
NC_000011.8:g.4069319C>T	NCBI36
NG_016277.1:g.240811C>T , LRG_164:g.240811C>T
NG_027992.2:g.1820C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*187C>T	ENSP00000432210.2:n.*187C>T
ENST00000698910.1:c.1284C>T	ENSP00000514024.1:p.Asp428=
ENST00000698911.1:c.1869C>T	ENSP00000514025.1:p.Asp623=
ENST00000698912.1:c.*187C>T	ENSP00000514026.1:n.*187C>T
ENST00000698913.1:c.1551C>T	ENSP00000514027.1:p.Asp517=
ENST00000698915.1:c.1857C>T	ENSP00000514029.1:p.Asp619=
ENST00000698916.1:c.1794C>T	ENSP00000514030.1:p.Asp598=
ENST00000698918.1:c.*1511C>T	ENSP00000514031.1:n.*1511C>T
ENST00000698919.1:c.*706C>T	ENSP00000514032.1:n.*706C>T
ENST00000698920.1:n.1073C>T
ENST00000526596.2:c.1866C>T MANE Select	ENSP00000433266.2:p.Asp622=
ENST00000300737.8:c.1773C>T	ENSP00000300737.4:p.Asp591=
ENST00000526156.1:n.571C>T
ENST00000526596.1:c.1058C>T
ENST00000527651.5:c.*187C>T	ENSP00000436208.1:n.*187C>T
ENST00000533977.5:c.1254C>T	ENSP00000434767.1:p.Asp418=
ENST00000616714.4:c.2091C>T	ENSP00000478059.1:p.Asp697=
NM_001277961.1:c.2091C>T	NP_001264890.1:p.Asp697=
NM_001277962.1:c.*187C>T	NP_001264891.1:n.*187C>T
NM_003156.3:c.1773C>T , LRG_164t1:c.1773C>T	NP_003147.2:p.Asp591=
NM_001277962.2:c.*187C>T	NP_001264891.1:n.*187C>T
NM_001277961.3:c.2091C>T	NP_001264890.1:p.Asp697=
NM_001382566.1:c.1869C>T	NP_001369495.1:p.Asp623=
NM_001382567.1:c.1866C>T MANE Select	NP_001369496.1:p.Asp622=
NM_001382568.1:c.1794C>T	NP_001369497.1:p.Asp598=
NM_001382569.1:c.1638C>T	NP_001369498.1:p.Asp546=
NM_001382570.1:c.1545C>T	NP_001369499.1:p.Asp515=
NM_001382571.1:c.1293C>T	NP_001369500.1:p.Asp431=
NM_001382575.1:c.1551C>T	NP_001369504.1:p.Asp517=
NM_001382576.1:c.1551C>T	NP_001369505.1:p.Asp517=
NM_001382577.1:c.1551C>T	NP_001369506.1:p.Asp517=
NM_001382578.1:c.*187C>T	NP_001369507.1:n.*187C>T
NM_001382579.1:c.*187C>T	NP_001369508.1:n.*187C>T
NM_001382580.1:c.*187C>T	NP_001369509.1:n.*187C>T
NM_001382581.1:c.1284C>T	NP_001369510.1:p.Asp428=
NM_003156.4:c.1773C>T	NP_003147.2:p.Asp591=
NR_168436.1:n.1697C>T
NR_168437.1:n.2202C>T
NR_168438.1:n.2024C>T