Canonical Allele Identifier: CA16607013

Gene: ATP2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28882548A>G , CM000678.2:g.28882548A>G	GRCh38
NC_000016.9:g.28893869A>G , CM000678.1:g.28893869A>G	GRCh37
NC_000016.8:g.28801370A>G	NCBI36
NG_023327.1:g.9061A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004320.6:c.422A>G MANE Select	NP_004311.1:p.Lys141Arg
ENST00000395503.9:c.422A>G MANE Select	ENSP00000378879.5:p.Lys141Arg
NM_001286075.1:c.47A>G	NP_001273004.1:p.Lys16Arg
NM_001286075.2:c.47A>G	NP_001273004.1:p.Lys16Arg
NM_004320.4:c.422A>G	NP_004311.1:p.Lys141Arg
NM_173201.3:c.422A>G	NP_775293.1:p.Lys141Arg
NM_173201.4:c.422A>G	NP_775293.1:p.Lys141Arg
NM_173201.5:c.422A>G	NP_775293.1:p.Lys141Arg
ENST00000357084.7:c.422A>G	ENSP00000349595.3:p.Lys141Arg
ENST00000395503.8:c.422A>G	ENSP00000378879.4:p.Lys141Arg
ENST00000536376.5:c.47A>G	ENSP00000443101.1:p.Lys16Arg
ENST00000562185.5:c.47A>G	ENSP00000457798.1:p.Lys16Arg
ENST00000563975.1:c.338A>G	ENSP00000458035.1:p.Lys113Arg