Canonical Allele Identifier: CA1261057256
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641278C= , CM000664.2:g.73641278C= GRCh38
NC_000002.11:g.73868405C= , CM000664.1:g.73868405C= GRCh37
NC_000002.10:g.73721913C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.351G= (NAT8) MANE Select ENSP00000272425.3:p.Lys117=
ENST00000652439.1:n.196C= (ALMS1P1)
ENST00000272425.3:c.351G= (NAT8) ENSP00000272425.3:p.Lys117=
NM_003960.3:c.351G= (NAT8) NP_003951.3:p.Lys117=
NM_003960.4:c.351G= (NAT8) MANE Select NP_003951.3:p.Lys117=