Canonical Allele Identifier: CA347287829
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Linked Data

dbSNP Id: rs540594336
gnomAD v2: 2-73868393-C-G
gnomAD v3: 2-73641266-C-G
gnomAD v4: 2-73641266-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641266C>G , CM000664.2:g.73641266C>G GRCh38
NC_000002.11:g.73868393C>G , CM000664.1:g.73868393C>G GRCh37
NC_000002.10:g.73721901C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.363G>C (NAT8) MANE Select ENSP00000272425.3:p.Met121Ile
ENST00000652439.1:n.184C>G (ALMS1P1)
ENST00000272425.3:c.363G>C (NAT8) ENSP00000272425.3:p.Met121Ile
NM_003960.3:c.363G>C (NAT8) NP_003951.3:p.Met121Ile
NM_003960.4:c.363G>C (NAT8) MANE Select NP_003951.3:p.Met121Ile