Canonical Allele Identifier: CA2062756805

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110292122C= , CM000674.2:g.110292122C=	GRCh38
NC_000012.11:g.110729927C= , CM000674.1:g.110729927C=	GRCh37
NC_000012.10:g.109214310C=	NCBI36
NG_007097.2:g.15496C=

Transcript Alleles

HGVS	Amino-acid Change
NM_170665.4:c.322C= MANE Select	NP_733765.1:p.Gln108=
ENST00000539276.7:c.322C= MANE Select	ENSP00000440045.2:p.Gln108=
NM_001681.3:c.322C=	NP_001672.1:p.Gln108=
NM_001681.4:c.322C=	NP_001672.1:p.Gln108=
NM_170665.3:c.322C=	NP_733765.1:p.Gln108=
ENST00000308664.10:c.322C=	ENSP00000311186.6:p.Gln108=
ENST00000377685.9:c.*162C=	ENSP00000366913.4:n.*162C=
ENST00000539276.6:c.322C=	ENSP00000440045.2:p.Gln108=
ENST00000548169.2:c.74C=
ENST00000552636.1:c.21C=	ENSP00000447406.1:p.Gly7=
ENST00000552636.2:c.-54C=	ENSP00000447406.2:n.-54C=
XM_005253888.1:c.322C=	XP_005253945.1:p.Gln108=
XM_005253888.3:c.322C=	XP_005253945.1:p.Gln108=
XM_011538402.1:c.322C=	XP_011536704.1:p.Gln108=
XM_011538402.3:c.322C=	XP_011536704.1:p.Gln108=
XM_011538403.1:c.322C=	XP_011536705.1:p.Gln108=
XR_002957329.1:n.328C=
XR_243009.1:n.328C=
XR_243009.3:n.328C=