Canonical Allele Identifier: CA6783574

Gene: ATP2A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110281870A>G , CM000674.2:g.110281870A>G	GRCh38
NC_000012.11:g.110719675A>G , CM000674.1:g.110719675A>G	GRCh37
NC_000012.10:g.109204058A>G	NCBI36
NG_007097.2:g.5244A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_170665.4:c.81A>G MANE Select	NP_733765.1:p.Glu27=
ENST00000539276.7:c.81A>G MANE Select	ENSP00000440045.2:p.Glu27=
NM_001681.3:c.81A>G	NP_001672.1:p.Glu27=
NM_001681.4:c.81A>G	NP_001672.1:p.Glu27=
NM_170665.3:c.81A>G	NP_733765.1:p.Glu27=
ENST00000308664.10:c.81A>G	ENSP00000311186.6:p.Glu27=
ENST00000377685.9:c.81A>G	ENSP00000366913.4:p.Glu27=
ENST00000539276.6:c.81A>G	ENSP00000440045.2:p.Glu27=
ENST00000552636.1:c.-183-734A>G	ENSP00000447406.1:n.-183-734A>G
ENST00000552636.2:c.-257-734A>G	ENSP00000447406.2:n.-257-734A>G
XM_005253888.1:c.81A>G	XP_005253945.1:p.Glu27=
XM_005253888.3:c.81A>G	XP_005253945.1:p.Glu27=
XM_011538402.1:c.81A>G	XP_011536704.1:p.Glu27=
XM_011538402.3:c.81A>G	XP_011536704.1:p.Glu27=
XM_011538403.1:c.81A>G	XP_011536705.1:p.Glu27=
XR_002957329.1:n.87A>G
XR_243009.1:n.87A>G
XR_243009.3:n.87A>G