Canonical Allele Identifier: CA347287484
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Linked Data

dbSNP Id: rs1229278175
gnomAD v2: 2-73868353-T-C
gnomAD v4: 2-73641226-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641226T>C , CM000664.2:g.73641226T>C GRCh38
NC_000002.11:g.73868353T>C , CM000664.1:g.73868353T>C GRCh37
NC_000002.10:g.73721861T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.403A>G (NAT8) MANE Select ENSP00000272425.3:p.Lys135Glu
ENST00000652439.1:n.144T>C (ALMS1P1)
ENST00000272425.3:c.403A>G (NAT8) ENSP00000272425.3:p.Lys135Glu
NM_003960.3:c.403A>G (NAT8) NP_003951.3:p.Lys135Glu
NM_003960.4:c.403A>G (NAT8) MANE Select NP_003951.3:p.Lys135Glu