Canonical Allele Identifier: CA1261057023
Gene: NAT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640868A= , CM000664.2:g.73640868A= GRCh38
NC_000002.11:g.73867995A= , CM000664.1:g.73867995A= GRCh37
NC_000002.10:g.73721503A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*77T= MANE Select ENSP00000272425.3:n.*77T=
ENST00000272425.3:c.*77T= ENSP00000272425.3:n.*77T=
NM_003960.3:c.*77T= NP_003951.3:n.*77T=
NM_003960.4:c.*77T= MANE Select NP_003951.3:n.*77T=