Canonical Allele Identifier: CA1768219138
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400763G= , CM000670.2:g.18400763G= GRCh38
NC_000008.10:g.18258273G= , CM000670.1:g.18258273G= GRCh37
NC_000008.9:g.18302553G= NCBI36
NG_012246.1:g.14519G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.760G= MANE Select ENSP00000286479.3:p.Glu254=
ENST00000286479.3:c.760G= ENSP00000286479.3:p.Glu254=
ENST00000520116.1:c.370G= ENSP00000428416.1:p.Glu124=
NM_000015.2:c.760G= NP_000006.2:p.Glu254=
XM_011544358.1:c.760G= XP_011542660.1:p.Glu254=
XM_017012938.1:c.760G= XP_016868427.1:p.Glu254=
NM_000015.3:c.760G= MANE Select NP_000006.2:p.Glu254=