Canonical Allele Identifier: CA2062809663

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345160G= , CM000674.2:g.110345160G=	GRCh38
NC_000012.11:g.110782965G= , CM000674.1:g.110782965G=	GRCh37
NC_000012.10:g.109267348G=	NCBI36
NG_007097.2:g.68534G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2608-89G= MANE Select	ENSP00000440045.2:n.2608-89G=
ENST00000308664.10:c.2608-89G=	ENSP00000311186.6:n.2608-89G=
ENST00000377685.9:c.*2448-89G=	ENSP00000366913.4:n.*2448-89G=
ENST00000539276.6:c.2608-89G=	ENSP00000440045.2:n.2608-89G=
ENST00000547792.1:n.454G=
ENST00000548169.2:c.2279-89G=
NM_001681.3:c.2608-89G=	NP_001672.1:n.2608-89G=
NM_170665.3:c.2608-89G=	NP_733765.1:n.2608-89G=
XM_005253888.1:c.2608-89G=	XP_005253945.1:n.2608-89G=
XM_011538402.1:c.2608-89G=	XP_011536704.1:n.2608-89G=
XR_243009.1:n.2614-89G=
XM_005253888.3:c.2608-89G=	XP_005253945.1:n.2608-89G=
XM_011538402.3:c.2608-89G=	XP_011536704.1:n.2608-89G=
XR_002957329.1:n.2614-89G=
XR_243009.3:n.2614-89G=
NM_170665.4:c.2608-89G= MANE Select	NP_733765.1:n.2608-89G=
NM_001681.4:c.2608-89G=	NP_001672.1:n.2608-89G=