Canonical Allele Identifier: CA379197271

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112730A>C (hg19) ; chr11:g.4091500A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091500A>C , CM000673.2:g.4091500A>C	GRCh38
NC_000011.9:g.4112730A>C , CM000673.1:g.4112730A>C	GRCh37
NC_000011.8:g.4069306A>C	NCBI36
NG_016277.1:g.240798A>C , LRG_164:g.240798A>C
NG_027992.2:g.1807A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*174A>C	ENSP00000432210.2:n.*174A>C
ENST00000698910.1:c.1271A>C	ENSP00000514024.1:p.Asn424Thr
ENST00000698911.1:c.1856A>C	ENSP00000514025.1:p.Asn619Thr
ENST00000698912.1:c.*174A>C	ENSP00000514026.1:n.*174A>C
ENST00000698913.1:c.1538A>C	ENSP00000514027.1:p.Asn513Thr
ENST00000698915.1:c.1844A>C	ENSP00000514029.1:p.Asn615Thr
ENST00000698916.1:c.1781A>C	ENSP00000514030.1:p.Asn594Thr
ENST00000698918.1:c.*1498A>C	ENSP00000514031.1:n.*1498A>C
ENST00000698919.1:c.*693A>C	ENSP00000514032.1:n.*693A>C
ENST00000698920.1:n.1060A>C
ENST00000526596.2:c.1853A>C MANE Select	ENSP00000433266.2:p.Asn618Thr
ENST00000300737.8:c.1760A>C	ENSP00000300737.4:p.Asn587Thr
ENST00000526156.1:n.558A>C
ENST00000526596.1:c.1045A>C
ENST00000527651.5:c.*174A>C	ENSP00000436208.1:n.*174A>C
ENST00000533977.5:c.1241A>C	ENSP00000434767.1:p.Asn414Thr
ENST00000616714.4:c.2078A>C	ENSP00000478059.1:p.Asn693Thr
NM_001277961.1:c.2078A>C	NP_001264890.1:p.Asn693Thr
NM_001277962.1:c.*174A>C	NP_001264891.1:n.*174A>C
NM_003156.3:c.1760A>C , LRG_164t1:c.1760A>C	NP_003147.2:p.Asn587Thr
NM_001277962.2:c.*174A>C	NP_001264891.1:n.*174A>C
NM_001277961.3:c.2078A>C	NP_001264890.1:p.Asn693Thr
NM_001382566.1:c.1856A>C	NP_001369495.1:p.Asn619Thr
NM_001382567.1:c.1853A>C MANE Select	NP_001369496.1:p.Asn618Thr
NM_001382568.1:c.1781A>C	NP_001369497.1:p.Asn594Thr
NM_001382569.1:c.1625A>C	NP_001369498.1:p.Asn542Thr
NM_001382570.1:c.1532A>C	NP_001369499.1:p.Asn511Thr
NM_001382571.1:c.1280A>C	NP_001369500.1:p.Asn427Thr
NM_001382575.1:c.1538A>C	NP_001369504.1:p.Asn513Thr
NM_001382576.1:c.1538A>C	NP_001369505.1:p.Asn513Thr
NM_001382577.1:c.1538A>C	NP_001369506.1:p.Asn513Thr
NM_001382578.1:c.*174A>C	NP_001369507.1:n.*174A>C
NM_001382579.1:c.*174A>C	NP_001369508.1:n.*174A>C
NM_001382580.1:c.*174A>C	NP_001369509.1:n.*174A>C
NM_001382581.1:c.1271A>C	NP_001369510.1:p.Asn424Thr
NM_003156.4:c.1760A>C	NP_003147.2:p.Asn587Thr
NR_168436.1:n.1684A>C
NR_168437.1:n.2189A>C
NR_168438.1:n.2011A>C