Canonical Allele Identifier: CA2062803639

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110339644G= , CM000674.2:g.110339644G=	GRCh38
NC_000012.11:g.110777449G= , CM000674.1:g.110777449G=	GRCh37
NC_000012.10:g.109261832G=	NCBI36
NG_007097.2:g.63018G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.1684G= MANE Select	ENSP00000440045.2:p.Ala562=
ENST00000308664.10:c.1684G=	ENSP00000311186.6:p.Ala562=
ENST00000377685.9:c.*1524G=	ENSP00000366913.4:n.*1524G=
ENST00000539276.6:c.1684G=	ENSP00000440045.2:p.Ala562=
ENST00000548169.2:c.1355G=
NM_001681.3:c.1684G=	NP_001672.1:p.Ala562=
NM_170665.3:c.1684G=	NP_733765.1:p.Ala562=
XM_005253888.1:c.1684G=	XP_005253945.1:p.Ala562=
XM_011538402.1:c.1684G=	XP_011536704.1:p.Ala562=
XM_011538403.1:c.1684G=	XP_011536705.1:p.Ala562=
XR_243009.1:n.1690G=
XM_005253888.3:c.1684G=	XP_005253945.1:p.Ala562=
XM_011538402.3:c.1684G=	XP_011536704.1:p.Ala562=
XR_002957329.1:n.1690G=
XR_243009.3:n.1690G=
NM_170665.4:c.1684G= MANE Select	NP_733765.1:p.Ala562=
NM_001681.4:c.1684G=	NP_001672.1:p.Ala562=