Canonical Allele Identifier: CA719740579

Gene: ATP2A1

Linked Data

• dbSNP Id: rs1392880643
• MyVariant Identifiers: chr16:g.28912306_28912307insGGGGCCCAGGGCCAG (hg19) ; chr16:g.28900985_28900986insGGGGCCCAGGGCCAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28900986_28901000dup , CM000678.2:g.28900986_28901000dup	GRCh38
NC_000016.9:g.28912307_28912321dup , CM000678.1:g.28912307_28912321dup	GRCh37
NC_000016.8:g.28819808_28819822dup	NCBI36
NG_023327.1:g.27499_27513dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395503.9:c.2100+70_2100+84dup MANE Select	ENSP00000378879.5:n.2100+70_2100+84dup
ENST00000357084.7:c.2100+70_2100+84dup	ENSP00000349595.3:n.2100+70_2100+84dup
ENST00000395503.8:c.2100+70_2100+84dup	ENSP00000378879.4:n.2100+70_2100+84dup
ENST00000536376.5:c.1725+70_1725+84dup	ENSP00000443101.1:n.1725+70_1725+84dup
NM_001286075.1:c.1725+70_1725+84dup	NP_001273004.1:n.1725+70_1725+84dup
NM_004320.4:c.2100+70_2100+84dup	NP_004311.1:n.2100+70_2100+84dup
NM_173201.3:c.2100+70_2100+84dup	NP_775293.1:n.2100+70_2100+84dup
NM_004320.6:c.2100+70_2100+84dup MANE Select	NP_004311.1:n.2100+70_2100+84dup
NM_173201.4:c.2100+70_2100+84dup	NP_775293.1:n.2100+70_2100+84dup
NM_001286075.2:c.1725+70_1725+84dup	NP_001273004.1:n.1725+70_1725+84dup
NM_173201.5:c.2100+70_2100+84dup	NP_775293.1:n.2100+70_2100+84dup