Canonical Allele Identifier: CA14115025

Gene: ATP10A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.25667192T>C , CM000677.2:g.25667192T>C	GRCh38
NC_000015.9:g.25912339T>C , CM000677.1:g.25912339T>C	GRCh37
NC_000015.8:g.23463432T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011521827.1:c.4351A>G	XP_011520129.1:p.Ile1451Val