Canonical Allele Identifier: CA1768219152
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400784G= , CM000670.2:g.18400784G= GRCh38
NC_000008.10:g.18258294G= , CM000670.1:g.18258294G= GRCh37
NC_000008.9:g.18302574G= NCBI36
NG_012246.1:g.14540G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.781G= MANE Select ENSP00000286479.3:p.Glu261=
ENST00000286479.3:c.781G= ENSP00000286479.3:p.Glu261=
ENST00000520116.1:c.391G= ENSP00000428416.1:p.Glu131=
NM_000015.2:c.781G= NP_000006.2:p.Glu261=
XM_011544358.1:c.781G= XP_011542660.1:p.Glu261=
XM_017012938.1:c.781G= XP_016868427.1:p.Glu261=
NM_000015.3:c.781G= MANE Select NP_000006.2:p.Glu261=