Canonical Allele Identifier: CA2062810474

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345641G= , CM000674.2:g.110345641G=	GRCh38
NC_000012.11:g.110783446G= , CM000674.1:g.110783446G=	GRCh37
NC_000012.10:g.109267829G=	NCBI36
NG_007097.2:g.69015G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2741+259G= MANE Select	ENSP00000440045.2:n.2741+259G=
ENST00000308664.10:c.2741+259G=	ENSP00000311186.6:n.2741+259G=
ENST00000313432.5:n.205G=
ENST00000377685.9:c.*2581+259G=	ENSP00000366913.4:n.*2581+259G=
ENST00000539276.6:c.2741+259G=	ENSP00000440045.2:n.2741+259G=
ENST00000548169.2:c.2412+259G=
NM_001681.3:c.2741+259G=	NP_001672.1:n.2741+259G=
NM_170665.3:c.2741+259G=	NP_733765.1:n.2741+259G=
XM_005253888.1:c.2741+259G=	XP_005253945.1:n.2741+259G=
XM_011538402.1:c.2741+259G=	XP_011536704.1:n.2741+259G=
XR_243009.1:n.2747+259G=
XM_005253888.3:c.2741+259G=	XP_005253945.1:n.2741+259G=
XM_011538402.3:c.2741+259G=	XP_011536704.1:n.2741+259G=
XR_002957329.1:n.2747+259G=
XR_243009.3:n.2747+259G=
NM_170665.4:c.2741+259G= MANE Select	NP_733765.1:n.2741+259G=
NM_001681.4:c.2741+259G=	NP_001672.1:n.2741+259G=