Canonical Allele Identifier: CA2238618343

Gene: ATP2C2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84412588G= , CM000678.2:g.84412588G=	GRCh38
NC_000016.9:g.84446194G= , CM000678.1:g.84446194G=	GRCh37
NC_000016.8:g.83003695G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262429.9:c.515+1823G= MANE Select	ENSP00000262429.4:n.515+1823G=
ENST00000262429.8:c.515+1823G=	ENSP00000262429.4:n.515+1823G=
ENST00000416219.6:c.515+1823G=	ENSP00000397925.2:n.515+1823G=
ENST00000420010.6:n.188+1985G=
ENST00000565546.5:n.250+1823G=
ENST00000565631.5:n.1006+1823G=
ENST00000565927.1:n.504+1823G=
ENST00000569207.5:c.237+1823G=
NM_001286527.2:c.515+1823G=	NP_001273456.2:n.515+1823G=
NM_001291454.1:c.62+1985G=	NP_001278383.1:n.62+1985G=
NM_014861.3:c.515+1823G=	NP_055676.3:n.515+1823G=
XM_011523486.1:c.446+1823G=	XP_011521788.1:n.446+1823G=
XM_011523486.2:c.446+1823G=	XP_011521788.1:n.446+1823G=
XR_001752045.1:n.608+1823G=
NM_001286527.3:c.515+1823G=	NP_001273456.2:n.515+1823G=
NM_001291454.2:c.62+1985G=	NP_001278383.1:n.62+1985G=
NM_014861.4:c.515+1823G= MANE Select	NP_055676.3:n.515+1823G=