Canonical Allele Identifier: CA2215889058
Gene: ATP2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28903068G= , CM000678.2:g.28903068G= GRCh38
NC_000016.9:g.28914389G= , CM000678.1:g.28914389G= GRCh37
NC_000016.8:g.28821890G= NCBI36
NG_023327.1:g.29581G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395503.9:c.2783G= MANE Select ENSP00000378879.5:p.Trp928=
ENST00000357084.7:c.2783G= ENSP00000349595.3:p.Trp928=
ENST00000395503.8:c.2783G= ENSP00000378879.4:p.Trp928=
ENST00000536376.5:c.2408G= ENSP00000443101.1:p.Trp803=
NM_001286075.1:c.2408G= NP_001273004.1:p.Trp803=
NM_004320.4:c.2783G= NP_004311.1:p.Trp928=
NM_173201.3:c.2783G= NP_775293.1:p.Trp928=
NM_004320.6:c.2783G= MANE Select NP_004311.1:p.Trp928=
NM_173201.4:c.2783G= NP_775293.1:p.Trp928=
NM_001286075.2:c.2408G= NP_001273004.1:p.Trp803=
NM_173201.5:c.2783G= NP_775293.1:p.Trp928=