Canonical Allele Identifier: CA1446055599

Gene: STIM2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.26999373A= , CM000666.2:g.26999373A=	GRCh38
NC_000004.11:g.27000995A= , CM000666.1:g.27000995A=	GRCh37
NC_000004.10:g.26610093A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698882.1:c.886+26A=	ENSP00000514004.1:n.886+26A=
ENST00000465503.6:c.625+26A=	ENSP00000417569.2:n.625+26A=
ENST00000467011.6:c.625+26A=	ENSP00000419383.2:n.625+26A=
ENST00000467087.7:c.625+26A= MANE Select	ENSP00000419073.2:n.625+26A=
ENST00000477474.3:c.466+26A=	ENSP00000419536.3:n.466+26A=
ENST00000463501.5:c.466+26A=	ENSP00000473283.1:n.466+26A=
ENST00000465503.5:c.625+26A=	ENSP00000417569.1:n.625+26A=
ENST00000467011.5:c.625+26A=	ENSP00000419383.1:n.625+26A=
ENST00000467087.5:c.625+26A=	ENSP00000419073.1:n.625+26A=
ENST00000494628.6:c.466+26A=	ENSP00000473527.1:n.466+26A=
NM_001169117.1:c.625+26A=	NP_001162588.1:n.625+26A=
NM_001169118.1:c.625+26A=	NP_001162589.1:n.625+26A=
NM_020860.3:c.625+26A=	NP_065911.3:n.625+26A=
NM_001169117.2:c.625+26A=	NP_001162588.1:n.625+26A=
NM_001169118.2:c.625+26A=	NP_001162589.1:n.625+26A=
NM_020860.4:c.625+26A= MANE Select	NP_065911.3:n.625+26A=