Canonical Allele Identifier: CA1261057051
Gene: NAT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640904G= , CM000664.2:g.73640904G= GRCh38
NC_000002.11:g.73868031G= , CM000664.1:g.73868031G= GRCh37
NC_000002.10:g.73721539G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*41C= MANE Select ENSP00000272425.3:n.*41C=
ENST00000272425.3:c.*41C= ENSP00000272425.3:n.*41C=
NM_003960.3:c.*41C= NP_003951.3:n.*41C=
NM_003960.4:c.*41C= MANE Select NP_003951.3:n.*41C=