Canonical Allele Identifier: CA2062803214

Gene: ATP2A2

Linked Data

• dbSNP Id: rs1879129915

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110339251dup , CM000674.2:g.110339251dup	GRCh38
NC_000012.11:g.110777056dup , CM000674.1:g.110777056dup	GRCh37
NC_000012.10:g.109261439dup	NCBI36
NG_007097.2:g.62625dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.1420-30dup MANE Select	ENSP00000440045.2:n.1420-30dup
ENST00000308664.10:c.1420-30dup	ENSP00000311186.6:n.1420-30dup
ENST00000377685.9:c.*1260-30dup	ENSP00000366913.4:n.*1260-30dup
ENST00000539276.6:c.1420-30dup	ENSP00000440045.2:n.1420-30dup
ENST00000548169.2:c.1091-30dup
NM_001681.3:c.1420-30dup	NP_001672.1:n.1420-30dup
NM_170665.3:c.1420-30dup	NP_733765.1:n.1420-30dup
XM_005253888.1:c.1420-30dup	XP_005253945.1:n.1420-30dup
XM_011538402.1:c.1420-30dup	XP_011536704.1:n.1420-30dup
XM_011538403.1:c.1420-30dup	XP_011536705.1:n.1420-30dup
XR_243009.1:n.1426-30dup
XM_005253888.3:c.1420-30dup	XP_005253945.1:n.1420-30dup
XM_011538402.3:c.1420-30dup	XP_011536704.1:n.1420-30dup
XR_002957329.1:n.1426-30dup
XR_243009.3:n.1426-30dup
NM_170665.4:c.1420-30dup MANE Select	NP_733765.1:n.1420-30dup
NM_001681.4:c.1420-30dup	NP_001672.1:n.1420-30dup