Canonical Allele Identifier: CA1261057211
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641199_73641201delinsCAA , CM000664.2:g.73641199_73641201delinsCAA GRCh38
NC_000002.11:g.73868326_73868328delinsCAA , CM000664.1:g.73868326_73868328delinsCAA GRCh37
NC_000002.10:g.73721834_73721836delinsCAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272425.4:c.428_430delinsTTG (NAT8) MANE Select ENSP00000272425.3:p.Phe143=
ENST00000652439.1:n.117_119delinsCAA (ALMS1P1)
ENST00000272425.3:c.428_430delinsTTG (NAT8) ENSP00000272425.3:p.Phe143=
NM_003960.3:c.428_430delinsTTG (NAT8) NP_003951.3:p.Phe143=
NM_003960.4:c.428_430delinsTTG (NAT8) MANE Select NP_003951.3:p.Phe143=