Canonical Allele Identifier: CA2620870501

Gene: ATP2A2

Linked Data

• gnomAD v4: 12-110345535-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345535C>A , CM000674.2:g.110345535C>A	GRCh38
NC_000012.11:g.110783340C>A , CM000674.1:g.110783340C>A	GRCh37
NC_000012.10:g.109267723C>A	NCBI36
NG_007097.2:g.68909C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2741+153C>A MANE Select	ENSP00000440045.2:n.2741+153C>A
ENST00000308664.10:c.2741+153C>A	ENSP00000311186.6:n.2741+153C>A
ENST00000313432.5:n.99C>A
ENST00000377685.9:c.*2581+153C>A	ENSP00000366913.4:n.*2581+153C>A
ENST00000539276.6:c.2741+153C>A	ENSP00000440045.2:n.2741+153C>A
ENST00000548169.2:c.2412+153C>A
NM_001681.3:c.2741+153C>A	NP_001672.1:n.2741+153C>A
NM_170665.3:c.2741+153C>A	NP_733765.1:n.2741+153C>A
XM_005253888.1:c.2741+153C>A	XP_005253945.1:n.2741+153C>A
XM_011538402.1:c.2741+153C>A	XP_011536704.1:n.2741+153C>A
XR_243009.1:n.2747+153C>A
XM_005253888.3:c.2741+153C>A	XP_005253945.1:n.2741+153C>A
XM_011538402.3:c.2741+153C>A	XP_011536704.1:n.2741+153C>A
XR_002957329.1:n.2747+153C>A
XR_243009.3:n.2747+153C>A
NM_170665.4:c.2741+153C>A MANE Select	NP_733765.1:n.2741+153C>A
NM_001681.4:c.2741+153C>A	NP_001672.1:n.2741+153C>A