Canonical Allele Identifier: CA347287058
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Linked Data

dbSNP Id: rs1676386371

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641121A>G , CM000664.2:g.73641121A>G GRCh38
NC_000002.11:g.73868248A>G , CM000664.1:g.73868248A>G GRCh37
NC_000002.10:g.73721756A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.508T>C (NAT8) MANE Select ENSP00000272425.3:p.Tyr170His
ENST00000652439.1:n.39A>G (ALMS1P1)
ENST00000272425.3:c.508T>C (NAT8) ENSP00000272425.3:p.Tyr170His
NM_003960.3:c.508T>C (NAT8) NP_003951.3:p.Tyr170His
NM_003960.4:c.508T>C (NAT8) MANE Select NP_003951.3:p.Tyr170His