Canonical Allele Identifier: CA472869676
Gene: STIM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.4112722G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4091492G>A , CM000673.2:g.4091492G>A GRCh38
NC_000011.9:g.4112722G>A , CM000673.1:g.4112722G>A GRCh37
NC_000011.8:g.4069298G>A NCBI36
NG_016277.1:g.240790G>A , LRG_164:g.240790G>A
NG_027992.2:g.1799G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525403.6:c.*166G>A ENSP00000432210.2:n.*166G>A
ENST00000698910.1:c.1263G>A ENSP00000514024.1:p.Leu421=
ENST00000698911.1:c.1848G>A ENSP00000514025.1:p.Leu616=
ENST00000698912.1:c.*166G>A ENSP00000514026.1:n.*166G>A
ENST00000698913.1:c.1530G>A ENSP00000514027.1:p.Leu510=
ENST00000698915.1:c.1836G>A ENSP00000514029.1:p.Leu612=
ENST00000698916.1:c.1773G>A ENSP00000514030.1:p.Leu591=
ENST00000698918.1:c.*1490G>A ENSP00000514031.1:n.*1490G>A
ENST00000698919.1:c.*685G>A ENSP00000514032.1:n.*685G>A
ENST00000698920.1:n.1052G>A
ENST00000526596.2:c.1845G>A MANE Select ENSP00000433266.2:p.Leu615=
ENST00000300737.8:c.1752G>A ENSP00000300737.4:p.Leu584=
ENST00000526156.1:n.550G>A
ENST00000526596.1:c.1037G>A
ENST00000527651.5:c.*166G>A ENSP00000436208.1:n.*166G>A
ENST00000533977.5:c.1233G>A ENSP00000434767.1:p.Leu411=
ENST00000616714.4:c.2070G>A ENSP00000478059.1:p.Leu690=
NM_001277961.1:c.2070G>A NP_001264890.1:p.Leu690=
NM_001277962.1:c.*166G>A NP_001264891.1:n.*166G>A
NM_003156.3:c.1752G>A , LRG_164t1:c.1752G>A NP_003147.2:p.Leu584=
NM_001277962.2:c.*166G>A NP_001264891.1:n.*166G>A
NM_001277961.3:c.2070G>A NP_001264890.1:p.Leu690=
NM_001382566.1:c.1848G>A NP_001369495.1:p.Leu616=
NM_001382567.1:c.1845G>A MANE Select NP_001369496.1:p.Leu615=
NM_001382568.1:c.1773G>A NP_001369497.1:p.Leu591=
NM_001382569.1:c.1617G>A NP_001369498.1:p.Leu539=
NM_001382570.1:c.1524G>A NP_001369499.1:p.Leu508=
NM_001382571.1:c.1272G>A NP_001369500.1:p.Leu424=
NM_001382575.1:c.1530G>A NP_001369504.1:p.Leu510=
NM_001382576.1:c.1530G>A NP_001369505.1:p.Leu510=
NM_001382577.1:c.1530G>A NP_001369506.1:p.Leu510=
NM_001382578.1:c.*166G>A NP_001369507.1:n.*166G>A
NM_001382579.1:c.*166G>A NP_001369508.1:n.*166G>A
NM_001382580.1:c.*166G>A NP_001369509.1:n.*166G>A
NM_001382581.1:c.1263G>A NP_001369510.1:p.Leu421=
NM_003156.4:c.1752G>A NP_003147.2:p.Leu584=
NR_168436.1:n.1676G>A
NR_168437.1:n.2181G>A
NR_168438.1:n.2003G>A