Canonical Allele Identifier: CA2620870600

Gene: ATP2A2

Linked Data

• gnomAD v4: 12-110345667-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110345669_110345670dup , CM000674.2:g.110345669_110345670dup	GRCh38
NC_000012.11:g.110783474_110783475dup , CM000674.1:g.110783474_110783475dup	GRCh37
NC_000012.10:g.109267857_109267858dup	NCBI36
NG_007097.2:g.69043_69044dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539276.7:c.2741+287_2741+288dup MANE Select	ENSP00000440045.2:n.2741+287_2741+288dup
ENST00000308664.10:c.2741+287_2741+288dup	ENSP00000311186.6:n.2741+287_2741+288dup
ENST00000313432.5:n.233_234dup
ENST00000377685.9:c.*2581+287_*2581+288dup	ENSP00000366913.4:n.*2581+287_*2581+288dup
ENST00000539276.6:c.2741+287_2741+288dup	ENSP00000440045.2:n.2741+287_2741+288dup
ENST00000548169.2:c.2412+287_2412+288dup
NM_001681.3:c.2741+287_2741+288dup	NP_001672.1:n.2741+287_2741+288dup
NM_170665.3:c.2741+287_2741+288dup	NP_733765.1:n.2741+287_2741+288dup
XM_005253888.1:c.2741+287_2741+288dup	XP_005253945.1:n.2741+287_2741+288dup
XM_011538402.1:c.2741+287_2741+288dup	XP_011536704.1:n.2741+287_2741+288dup
XR_243009.1:n.2747+287_2747+288dup
XM_005253888.3:c.2741+287_2741+288dup	XP_005253945.1:n.2741+287_2741+288dup
XM_011538402.3:c.2741+287_2741+288dup	XP_011536704.1:n.2741+287_2741+288dup
XR_002957329.1:n.2747+287_2747+288dup
XR_243009.3:n.2747+287_2747+288dup
NM_170665.4:c.2741+287_2741+288dup MANE Select	NP_733765.1:n.2741+287_2741+288dup
NM_001681.4:c.2741+287_2741+288dup	NP_001672.1:n.2741+287_2741+288dup