Canonical Allele Identifier: CA347287408
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Linked Data

dbSNP Id: rs1315089099
gnomAD v2: 2-73868337-A-C
gnomAD v4: 2-73641210-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641210A>C , CM000664.2:g.73641210A>C GRCh38
NC_000002.11:g.73868337A>C , CM000664.1:g.73868337A>C GRCh37
NC_000002.10:g.73721845A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.419T>G (NAT8) MANE Select ENSP00000272425.3:p.Phe140Cys
ENST00000652439.1:n.128A>C (ALMS1P1)
ENST00000272425.3:c.419T>G (NAT8) ENSP00000272425.3:p.Phe140Cys
NM_003960.3:c.419T>G (NAT8) NP_003951.3:p.Phe140Cys
NM_003960.4:c.419T>G (NAT8) MANE Select NP_003951.3:p.Phe140Cys