Canonical Allele Identifier: CA2215888652

Gene: ATP2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28902899A= , CM000678.2:g.28902899A=	GRCh38
NC_000016.9:g.28914220A= , CM000678.1:g.28914220A=	GRCh37
NC_000016.8:g.28821721A=	NCBI36
NG_023327.1:g.29412A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395503.9:c.2732A= MANE Select	ENSP00000378879.5:p.Asn911=
ENST00000357084.7:c.2732A=	ENSP00000349595.3:p.Asn911=
ENST00000395503.8:c.2732A=	ENSP00000378879.4:p.Asn911=
ENST00000536376.5:c.2357A=	ENSP00000443101.1:p.Asn786=
NM_001286075.1:c.2357A=	NP_001273004.1:p.Asn786=
NM_004320.4:c.2732A=	NP_004311.1:p.Asn911=
NM_173201.3:c.2732A=	NP_775293.1:p.Asn911=
NM_004320.6:c.2732A= MANE Select	NP_004311.1:p.Asn911=
NM_173201.4:c.2732A=	NP_775293.1:p.Asn911=
NM_001286075.2:c.2357A=	NP_001273004.1:p.Asn786=
NM_173201.5:c.2732A=	NP_775293.1:p.Asn911=