Canonical Allele Identifier: CA2838418181

Gene: STIM2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.27006856T>A , CM000666.2:g.27006856T>A	GRCh38
NC_000004.11:g.27008478T>A , CM000666.1:g.27008478T>A	GRCh37
NC_000004.10:g.26617576T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698882.1:c.1243-677T>A	ENSP00000514004.1:n.1243-677T>A
ENST00000465503.6:c.982-677T>A	ENSP00000417569.2:n.982-677T>A
ENST00000467011.6:c.982-677T>A	ENSP00000419383.2:n.982-677T>A
ENST00000467087.7:c.982-677T>A MANE Select	ENSP00000419073.2:n.982-677T>A
ENST00000477474.3:c.823-677T>A	ENSP00000419536.3:n.823-677T>A
ENST00000465503.5:c.982-677T>A	ENSP00000417569.1:n.982-677T>A
ENST00000467011.5:c.982-677T>A	ENSP00000419383.1:n.982-677T>A
ENST00000467087.5:c.982-677T>A	ENSP00000419073.1:n.982-677T>A
ENST00000473519.5:c.106-677T>A	ENSP00000420113.1:n.106-677T>A
NM_001169117.1:c.982-677T>A	NP_001162588.1:n.982-677T>A
NM_001169118.1:c.982-677T>A	NP_001162589.1:n.982-677T>A
NM_020860.3:c.982-677T>A	NP_065911.3:n.982-677T>A
NM_001169117.2:c.982-677T>A	NP_001162588.1:n.982-677T>A
NM_001169118.2:c.982-677T>A	NP_001162589.1:n.982-677T>A
NM_020860.4:c.982-677T>A MANE Select	NP_065911.3:n.982-677T>A