Canonical Allele Identifier: CA2620866156

Gene: ATP2A2

Linked Data

• gnomAD v4: 12-110282823-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110282823C>A , CM000674.2:g.110282823C>A	GRCh38
NC_000012.11:g.110720628C>A , CM000674.1:g.110720628C>A	GRCh37
NC_000012.10:g.109205011C>A	NCBI36
NG_007097.2:g.6197C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000552636.2:c.-157+28C>A	ENSP00000447406.2:n.-157+28C>A
ENST00000539276.7:c.219+28C>A MANE Select	ENSP00000440045.2:n.219+28C>A
ENST00000308664.10:c.219+28C>A	ENSP00000311186.6:n.219+28C>A
ENST00000377685.9:c.*59+28C>A	ENSP00000366913.4:n.*59+28C>A
ENST00000539276.6:c.219+28C>A	ENSP00000440045.2:n.219+28C>A
ENST00000552636.1:c.-83+28C>A	ENSP00000447406.1:n.-83+28C>A
NM_001681.3:c.219+28C>A	NP_001672.1:n.219+28C>A
NM_170665.3:c.219+28C>A	NP_733765.1:n.219+28C>A
XM_005253888.1:c.219+28C>A	XP_005253945.1:n.219+28C>A
XM_011538402.1:c.219+28C>A	XP_011536704.1:n.219+28C>A
XM_011538403.1:c.219+28C>A	XP_011536705.1:n.219+28C>A
XR_243009.1:n.225+28C>A
XM_005253888.3:c.219+28C>A	XP_005253945.1:n.219+28C>A
XM_011538402.3:c.219+28C>A	XP_011536704.1:n.219+28C>A
XR_002957329.1:n.225+28C>A
XR_243009.3:n.225+28C>A
NM_170665.4:c.219+28C>A MANE Select	NP_733765.1:n.219+28C>A
NM_001681.4:c.219+28C>A	NP_001672.1:n.219+28C>A