Canonical Allele Identifier: CA494874485
Gene: ATP2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1596688646
MyVariant Identifiers: chr16:g.28914384A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28903063A>C , CM000678.2:g.28903063A>C GRCh38
NC_000016.9:g.28914384A>C , CM000678.1:g.28914384A>C GRCh37
NC_000016.8:g.28821885A>C NCBI36
NG_023327.1:g.29576A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395503.9:c.2778A>C MANE Select ENSP00000378879.5:p.Pro926=
ENST00000357084.7:c.2778A>C ENSP00000349595.3:p.Pro926=
ENST00000395503.8:c.2778A>C ENSP00000378879.4:p.Pro926=
ENST00000536376.5:c.2403A>C ENSP00000443101.1:p.Pro801=
NM_001286075.1:c.2403A>C NP_001273004.1:p.Pro801=
NM_004320.4:c.2778A>C NP_004311.1:p.Pro926=
NM_173201.3:c.2778A>C NP_775293.1:p.Pro926=
NM_004320.6:c.2778A>C MANE Select NP_004311.1:p.Pro926=
NM_173201.4:c.2778A>C NP_775293.1:p.Pro926=
NM_001286075.2:c.2403A>C NP_001273004.1:p.Pro801=
NM_173201.5:c.2778A>C NP_775293.1:p.Pro926=