Canonical Allele Identifier: CA1261057037
Gene: NAT8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640886G= , CM000664.2:g.73640886G= GRCh38
NC_000002.11:g.73868013G= , CM000664.1:g.73868013G= GRCh37
NC_000002.10:g.73721521G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*59C= MANE Select ENSP00000272425.3:n.*59C=
ENST00000272425.3:c.*59C= ENSP00000272425.3:n.*59C=
NM_003960.3:c.*59C= NP_003951.3:n.*59C=
NM_003960.4:c.*59C= MANE Select NP_003951.3:n.*59C=
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