Canonical Allele Identifier: CA1261057030
Gene: NAT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640879A= , CM000664.2:g.73640879A= GRCh38
NC_000002.11:g.73868006A= , CM000664.1:g.73868006A= GRCh37
NC_000002.10:g.73721514A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*66T= MANE Select ENSP00000272425.3:n.*66T=
ENST00000272425.3:c.*66T= ENSP00000272425.3:n.*66T=
NM_003960.3:c.*66T= NP_003951.3:n.*66T=
NM_003960.4:c.*66T= MANE Select NP_003951.3:n.*66T=