Canonical Allele Identifier: CA1261057129
Gene: NAT8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641041C= , CM000664.2:g.73641041C= GRCh38
NC_000002.11:g.73868168C= , CM000664.1:g.73868168C= GRCh37
NC_000002.10:g.73721676C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.588G= MANE Select ENSP00000272425.3:p.Thr196=
ENST00000272425.3:c.588G= ENSP00000272425.3:p.Thr196=
NM_003960.3:c.588G= NP_003951.3:p.Thr196=
NM_003960.4:c.588G= MANE Select NP_003951.3:p.Thr196=
Search 100 bp 5'
Search 100 bp 3'