Canonical Allele Identifier: CA379197320

Gene: STIM1

Linked Data

• MyVariant Identifiers: chr11:g.4112742A>C (hg19) ; chr11:g.4091512A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4091512A>C , CM000673.2:g.4091512A>C	GRCh38
NC_000011.9:g.4112742A>C , CM000673.1:g.4112742A>C	GRCh37
NC_000011.8:g.4069318A>C	NCBI36
NG_016277.1:g.240810A>C , LRG_164:g.240810A>C
NG_027992.2:g.1819A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525403.6:c.*186A>C	ENSP00000432210.2:n.*186A>C
ENST00000698910.1:c.1283A>C	ENSP00000514024.1:p.Asp428Ala
ENST00000698911.1:c.1868A>C	ENSP00000514025.1:p.Asp623Ala
ENST00000698912.1:c.*186A>C	ENSP00000514026.1:n.*186A>C
ENST00000698913.1:c.1550A>C	ENSP00000514027.1:p.Asp517Ala
ENST00000698915.1:c.1856A>C	ENSP00000514029.1:p.Asp619Ala
ENST00000698916.1:c.1793A>C	ENSP00000514030.1:p.Asp598Ala
ENST00000698918.1:c.*1510A>C	ENSP00000514031.1:n.*1510A>C
ENST00000698919.1:c.*705A>C	ENSP00000514032.1:n.*705A>C
ENST00000698920.1:n.1072A>C
ENST00000526596.2:c.1865A>C MANE Select	ENSP00000433266.2:p.Asp622Ala
ENST00000300737.8:c.1772A>C	ENSP00000300737.4:p.Asp591Ala
ENST00000526156.1:n.570A>C
ENST00000526596.1:c.1057A>C
ENST00000527651.5:c.*186A>C	ENSP00000436208.1:n.*186A>C
ENST00000533977.5:c.1253A>C	ENSP00000434767.1:p.Asp418Ala
ENST00000616714.4:c.2090A>C	ENSP00000478059.1:p.Asp697Ala
NM_001277961.1:c.2090A>C	NP_001264890.1:p.Asp697Ala
NM_001277962.1:c.*186A>C	NP_001264891.1:n.*186A>C
NM_003156.3:c.1772A>C , LRG_164t1:c.1772A>C	NP_003147.2:p.Asp591Ala
NM_001277962.2:c.*186A>C	NP_001264891.1:n.*186A>C
NM_001277961.3:c.2090A>C	NP_001264890.1:p.Asp697Ala
NM_001382566.1:c.1868A>C	NP_001369495.1:p.Asp623Ala
NM_001382567.1:c.1865A>C MANE Select	NP_001369496.1:p.Asp622Ala
NM_001382568.1:c.1793A>C	NP_001369497.1:p.Asp598Ala
NM_001382569.1:c.1637A>C	NP_001369498.1:p.Asp546Ala
NM_001382570.1:c.1544A>C	NP_001369499.1:p.Asp515Ala
NM_001382571.1:c.1292A>C	NP_001369500.1:p.Asp431Ala
NM_001382575.1:c.1550A>C	NP_001369504.1:p.Asp517Ala
NM_001382576.1:c.1550A>C	NP_001369505.1:p.Asp517Ala
NM_001382577.1:c.1550A>C	NP_001369506.1:p.Asp517Ala
NM_001382578.1:c.*186A>C	NP_001369507.1:n.*186A>C
NM_001382579.1:c.*186A>C	NP_001369508.1:n.*186A>C
NM_001382580.1:c.*186A>C	NP_001369509.1:n.*186A>C
NM_001382581.1:c.1283A>C	NP_001369510.1:p.Asp428Ala
NM_003156.4:c.1772A>C	NP_003147.2:p.Asp591Ala
NR_168436.1:n.1696A>C
NR_168437.1:n.2201A>C
NR_168438.1:n.2023A>C