Canonical Allele Identifier: CA481868251

Gene: ATP2A2

Linked Data

• gnomAD v4: 12-110339637-A-T
• MyVariant Identifiers: chr12:g.110777442A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110339637A>T , CM000674.2:g.110339637A>T	GRCh38
NC_000012.11:g.110777442A>T , CM000674.1:g.110777442A>T	GRCh37
NC_000012.10:g.109261825A>T	NCBI36
NG_007097.2:g.63011A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.1677A>T MANE Select	ENSP00000440045.2:p.Arg559=
ENST00000308664.10:c.1677A>T	ENSP00000311186.6:p.Arg559=
ENST00000377685.9:c.*1517A>T	ENSP00000366913.4:n.*1517A>T
ENST00000539276.6:c.1677A>T	ENSP00000440045.2:p.Arg559=
ENST00000548169.2:c.1348A>T
NM_001681.3:c.1677A>T	NP_001672.1:p.Arg559=
NM_170665.3:c.1677A>T	NP_733765.1:p.Arg559=
XM_005253888.1:c.1677A>T	XP_005253945.1:p.Arg559=
XM_011538402.1:c.1677A>T	XP_011536704.1:p.Arg559=
XM_011538403.1:c.1677A>T	XP_011536705.1:p.Arg559=
XR_243009.1:n.1683A>T
XM_005253888.3:c.1677A>T	XP_005253945.1:p.Arg559=
XM_011538402.3:c.1677A>T	XP_011536704.1:p.Arg559=
XR_002957329.1:n.1683A>T
XR_243009.3:n.1683A>T
NM_170665.4:c.1677A>T MANE Select	NP_733765.1:p.Arg559=
NM_001681.4:c.1677A>T	NP_001672.1:p.Arg559=