Canonical Allele Identifier: CA2830536851
Gene: ATP10D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47536080A>C , CM000666.2:g.47536080A>C GRCh38
NC_000004.11:g.47538097A>C , CM000666.1:g.47538097A>C GRCh37
NC_000004.10:g.47232854A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273859.8:c.1015+47A>C MANE Select ENSP00000273859.3:n.1015+47A>C
ENST00000273859.7:c.1015+47A>C ENSP00000273859.3:n.1015+47A>C
ENST00000504445.1:c.1015+47A>C ENSP00000420909.1:n.1015+47A>C
NM_020453.3:c.1015+47A>C NP_065186.3:n.1015+47A>C
XM_005248119.3:c.1015+47A>C XP_005248176.1:n.1015+47A>C
XM_005248120.3:c.1015+47A>C XP_005248177.1:n.1015+47A>C
XM_011513722.1:c.820+47A>C XP_011512024.1:n.820+47A>C
XR_925154.1:n.1301+47A>C
XM_005248119.4:c.1015+47A>C XP_005248176.1:n.1015+47A>C
XM_005248120.4:c.1015+47A>C XP_005248177.1:n.1015+47A>C
XM_011513722.2:c.820+47A>C XP_011512024.1:n.820+47A>C
XM_017008472.1:c.-571+47A>C XP_016863961.1:n.-571+47A>C
XR_001741295.1:n.1311+47A>C
XR_925154.2:n.1297+47A>C
NM_020453.4:c.1015+47A>C MANE Select NP_065186.3:n.1015+47A>C
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