Canonical Allele Identifier: CA472869692

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112740G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091510G>A , CM000673.2:g.4091510G>A	GRCh38
NC_000011.9:g.4112740G>A , CM000673.1:g.4112740G>A	GRCh37
NC_000011.8:g.4069316G>A	NCBI36
NG_016277.1:g.240808G>A , LRG_164:g.240808G>A
NG_027992.2:g.1817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*184G>A	ENSP00000432210.2:n.*184G>A
ENST00000698910.1:c.1281G>A	ENSP00000514024.1:p.Leu427=
ENST00000698911.1:c.1866G>A	ENSP00000514025.1:p.Leu622=
ENST00000698912.1:c.*184G>A	ENSP00000514026.1:n.*184G>A
ENST00000698913.1:c.1548G>A	ENSP00000514027.1:p.Leu516=
ENST00000698915.1:c.1854G>A	ENSP00000514029.1:p.Leu618=
ENST00000698916.1:c.1791G>A	ENSP00000514030.1:p.Leu597=
ENST00000698918.1:c.*1508G>A	ENSP00000514031.1:n.*1508G>A
ENST00000698919.1:c.*703G>A	ENSP00000514032.1:n.*703G>A
ENST00000698920.1:n.1070G>A
ENST00000526596.2:c.1863G>A MANE Select	ENSP00000433266.2:p.Leu621=
ENST00000300737.8:c.1770G>A	ENSP00000300737.4:p.Leu590=
ENST00000526156.1:n.568G>A
ENST00000526596.1:c.1055G>A
ENST00000527651.5:c.*184G>A	ENSP00000436208.1:n.*184G>A
ENST00000533977.5:c.1251G>A	ENSP00000434767.1:p.Leu417=
ENST00000616714.4:c.2088G>A	ENSP00000478059.1:p.Leu696=
NM_001277961.1:c.2088G>A	NP_001264890.1:p.Leu696=
NM_001277962.1:c.*184G>A	NP_001264891.1:n.*184G>A
NM_003156.3:c.1770G>A , LRG_164t1:c.1770G>A	NP_003147.2:p.Leu590=
NM_001277962.2:c.*184G>A	NP_001264891.1:n.*184G>A
NM_001277961.3:c.2088G>A	NP_001264890.1:p.Leu696=
NM_001382566.1:c.1866G>A	NP_001369495.1:p.Leu622=
NM_001382567.1:c.1863G>A MANE Select	NP_001369496.1:p.Leu621=
NM_001382568.1:c.1791G>A	NP_001369497.1:p.Leu597=
NM_001382569.1:c.1635G>A	NP_001369498.1:p.Leu545=
NM_001382570.1:c.1542G>A	NP_001369499.1:p.Leu514=
NM_001382571.1:c.1290G>A	NP_001369500.1:p.Leu430=
NM_001382575.1:c.1548G>A	NP_001369504.1:p.Leu516=
NM_001382576.1:c.1548G>A	NP_001369505.1:p.Leu516=
NM_001382577.1:c.1548G>A	NP_001369506.1:p.Leu516=
NM_001382578.1:c.*184G>A	NP_001369507.1:n.*184G>A
NM_001382579.1:c.*184G>A	NP_001369508.1:n.*184G>A
NM_001382580.1:c.*184G>A	NP_001369509.1:n.*184G>A
NM_001382581.1:c.1281G>A	NP_001369510.1:p.Leu427=
NM_003156.4:c.1770G>A	NP_003147.2:p.Leu590=
NR_168436.1:n.1694G>A
NR_168437.1:n.2199G>A
NR_168438.1:n.2021G>A