Canonical Allele Identifier: CA2695217312

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110340923dup , CM000674.2:g.110340923dup	GRCh38
NC_000012.11:g.110778728dup , CM000674.1:g.110778728dup	GRCh37
NC_000012.10:g.109263111dup	NCBI36
NG_007097.2:g.64297dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2026dup MANE Select	ENSP00000440045.2:p.Ala676GlyfsTer4
ENST00000308664.10:c.2026dup	ENSP00000311186.6:p.Ala676GlyfsTer4
ENST00000377685.9:c.*1866dup	ENSP00000366913.4:n.*1866dup
ENST00000539276.6:c.2026dup	ENSP00000440045.2:p.Ala676GlyfsTer4
ENST00000548169.2:c.1697dup
NM_001681.3:c.2026dup	NP_001672.1:p.Ala676GlyfsTer4
NM_170665.3:c.2026dup	NP_733765.1:p.Ala676GlyfsTer4
XM_005253888.1:c.2026dup	XP_005253945.1:p.Ala676GlyfsTer4
XM_011538402.1:c.2026dup	XP_011536704.1:p.Ala676GlyfsTer4
XM_011538403.1:c.2026dup	XP_011536705.1:p.Ala676GlyfsTer4
XR_243009.1:n.2032dup
XM_005253888.3:c.2026dup	XP_005253945.1:p.Ala676GlyfsTer4
XM_011538402.3:c.2026dup	XP_011536704.1:p.Ala676GlyfsTer4
XR_002957329.1:n.2032dup
XR_243009.3:n.2032dup
NM_170665.4:c.2026dup MANE Select	NP_733765.1:p.Ala676GlyfsTer4
NM_001681.4:c.2026dup	NP_001672.1:p.Ala676GlyfsTer4