Canonical Allele Identifier: CA1715707
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Linked Data

dbSNP Id: rs751488221
gnomAD v2: 2-73868333-A-G
gnomAD v4: 2-73641206-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641206A>G , CM000664.2:g.73641206A>G GRCh38
NC_000002.11:g.73868333A>G , CM000664.1:g.73868333A>G GRCh37
NC_000002.10:g.73721841A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272425.4:c.423T>C (NAT8) MANE Select ENSP00000272425.3:p.His141=
ENST00000652439.1:n.124A>G (ALMS1P1)
ENST00000272425.3:c.423T>C (NAT8) ENSP00000272425.3:p.His141=
NM_003960.3:c.423T>C (NAT8) NP_003951.3:p.His141=
NM_003960.4:c.423T>C (NAT8) MANE Select NP_003951.3:p.His141=