Canonical Allele Identifier: CA1452819098
Gene: ATP8A1 HGNC NCBI

Linked Data

dbSNP Id: rs12639920

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42410670T>C , CM000666.2:g.42410670T>C GRCh38
NC_000004.11:g.42412687T>C , CM000666.1:g.42412687T>C GRCh37
NC_000004.10:g.42107444T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000700470.1:c.*2246A>G ENSP00000515003.1:n.*2246A>G
ENST00000264449.14:c.*2246A>G ENSP00000264449.10:n.*2246A>G
ENST00000381668.9:c.*2246A>G MANE Select ENSP00000371084.5:n.*2246A>G
ENST00000514372.5:c.3621A>G ENSP00000426495.1:n.3621A>G
NM_001105529.1:c.*2246A>G NP_001098999.1:n.*2246A>G
NM_006095.2:c.*2246A>G MANE Select NP_006086.1:n.*2246A>G
XM_005248043.2:c.*2246A>G XP_005248100.1:n.*2246A>G
XM_011513615.1:c.*2246A>G XP_011511917.1:n.*2246A>G
XM_011513616.1:c.*2246A>G XP_011511918.1:n.*2246A>G
XM_011513618.1:c.*2246A>G XP_011511920.1:n.*2246A>G
XM_011513619.1:c.*2246A>G XP_011511921.1:n.*2246A>G
XR_925118.1:n.5795A>G
XM_005248043.3:c.*2246A>G XP_005248100.1:n.*2246A>G
XM_011513615.2:c.*2246A>G XP_011511917.1:n.*2246A>G
XM_011513616.3:c.*2246A>G XP_011511918.1:n.*2246A>G
XM_011513618.2:c.*2246A>G XP_011511920.1:n.*2246A>G
XM_017007645.2:c.*2246A>G XP_016863134.1:n.*2246A>G
XM_017007646.1:c.*2246A>G XP_016863135.1:n.*2246A>G
XM_017007647.1:c.*2246A>G XP_016863136.1:n.*2246A>G
XR_001741094.2:n.5814A>G
XR_925117.3:n.6008A>G
XR_925118.2:n.5800A>G
NM_001400024.1:c.*2246A>G NP_001386953.1:n.*2246A>G
NM_001400025.1:c.*2246A>G NP_001386954.1:n.*2246A>G
NM_001400026.1:c.*2246A>G NP_001386955.1:n.*2246A>G
NM_001400027.1:c.*2246A>G NP_001386956.1:n.*2246A>G