Canonical Allele Identifier: CA2062790143

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110282820T= , CM000674.2:g.110282820T=	GRCh38
NC_000012.11:g.110720625T= , CM000674.1:g.110720625T=	GRCh37
NC_000012.10:g.109205008T=	NCBI36
NG_007097.2:g.6194T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000552636.2:c.-157+25T=	ENSP00000447406.2:n.-157+25T=
ENST00000539276.7:c.219+25T= MANE Select	ENSP00000440045.2:n.219+25T=
ENST00000308664.10:c.219+25T=	ENSP00000311186.6:n.219+25T=
ENST00000377685.9:c.*59+25T=	ENSP00000366913.4:n.*59+25T=
ENST00000539276.6:c.219+25T=	ENSP00000440045.2:n.219+25T=
ENST00000552636.1:c.-83+25T=	ENSP00000447406.1:n.-83+25T=
NM_001681.3:c.219+25T=	NP_001672.1:n.219+25T=
NM_170665.3:c.219+25T=	NP_733765.1:n.219+25T=
XM_005253888.1:c.219+25T=	XP_005253945.1:n.219+25T=
XM_011538402.1:c.219+25T=	XP_011536704.1:n.219+25T=
XM_011538403.1:c.219+25T=	XP_011536705.1:n.219+25T=
XR_243009.1:n.225+25T=
XM_005253888.3:c.219+25T=	XP_005253945.1:n.219+25T=
XM_011538402.3:c.219+25T=	XP_011536704.1:n.219+25T=
XR_002957329.1:n.225+25T=
XR_243009.3:n.225+25T=
NM_170665.4:c.219+25T= MANE Select	NP_733765.1:n.219+25T=
NM_001681.4:c.219+25T=	NP_001672.1:n.219+25T=