Canonical Allele Identifier: CA494874490

Gene: ATP2A1

Linked Data

• MyVariant Identifiers: chr16:g.28914387C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28903066C>G , CM000678.2:g.28903066C>G	GRCh38
NC_000016.9:g.28914387C>G , CM000678.1:g.28914387C>G	GRCh37
NC_000016.8:g.28821888C>G	NCBI36
NG_023327.1:g.29579C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395503.9:c.2781C>G MANE Select	ENSP00000378879.5:p.Pro927=
ENST00000357084.7:c.2781C>G	ENSP00000349595.3:p.Pro927=
ENST00000395503.8:c.2781C>G	ENSP00000378879.4:p.Pro927=
ENST00000536376.5:c.2406C>G	ENSP00000443101.1:p.Pro802=
NM_001286075.1:c.2406C>G	NP_001273004.1:p.Pro802=
NM_004320.4:c.2781C>G	NP_004311.1:p.Pro927=
NM_173201.3:c.2781C>G	NP_775293.1:p.Pro927=
NM_004320.6:c.2781C>G MANE Select	NP_004311.1:p.Pro927=
NM_173201.4:c.2781C>G	NP_775293.1:p.Pro927=
NM_001286075.2:c.2406C>G	NP_001273004.1:p.Pro802=
NM_173201.5:c.2781C>G	NP_775293.1:p.Pro927=