Canonical Allele Identifier: CA395411528
Gene: ATP2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28900884T>C , CM000678.2:g.28900884T>C GRCh38
NC_000016.9:g.28912205T>C , CM000678.1:g.28912205T>C GRCh37
NC_000016.8:g.28819706T>C NCBI36
NG_023327.1:g.27397T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395503.9:c.2068T>C MANE Select ENSP00000378879.5:p.Tyr690His
ENST00000357084.7:c.2068T>C ENSP00000349595.3:p.Tyr690His
ENST00000395503.8:c.2068T>C ENSP00000378879.4:p.Tyr690His
ENST00000536376.5:c.1693T>C ENSP00000443101.1:p.Tyr565His
NM_001286075.1:c.1693T>C NP_001273004.1:p.Tyr565His
NM_004320.4:c.2068T>C NP_004311.1:p.Tyr690His
NM_173201.3:c.2068T>C NP_775293.1:p.Tyr690His
NM_004320.6:c.2068T>C MANE Select NP_004311.1:p.Tyr690His
NM_173201.4:c.2068T>C NP_775293.1:p.Tyr690His
NM_001286075.2:c.1693T>C NP_001273004.1:p.Tyr565His
NM_173201.5:c.2068T>C NP_775293.1:p.Tyr690His