Canonical Allele Identifier: CA1768218893
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400256C= , CM000670.2:g.18400256C= GRCh38
NC_000008.10:g.18257766C= , CM000670.1:g.18257766C= GRCh37
NC_000008.9:g.18302046C= NCBI36
NG_012246.1:g.14012C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.253C= MANE Select ENSP00000286479.3:p.Gln85=
ENST00000286479.3:c.253C= ENSP00000286479.3:p.Gln85=
ENST00000520116.1:c.-57-81C= ENSP00000428416.1:n.-57-81C=
NM_000015.2:c.253C= NP_000006.2:p.Gln85=
XM_011544358.1:c.253C= XP_011542660.1:p.Gln85=
XM_017012938.1:c.253C= XP_016868427.1:p.Gln85=
NM_000015.3:c.253C= MANE Select NP_000006.2:p.Gln85=