Canonical Allele Identifier: CA1768219151
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400783G= , CM000670.2:g.18400783G= GRCh38
NC_000008.10:g.18258293G= , CM000670.1:g.18258293G= GRCh37
NC_000008.9:g.18302573G= NCBI36
NG_012246.1:g.14539G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.780G= MANE Select ENSP00000286479.3:p.Glu260=
ENST00000286479.3:c.780G= ENSP00000286479.3:p.Glu260=
ENST00000520116.1:c.390G= ENSP00000428416.1:p.Glu130=
NM_000015.2:c.780G= NP_000006.2:p.Glu260=
XM_011544358.1:c.780G= XP_011542660.1:p.Glu260=
XM_017012938.1:c.780G= XP_016868427.1:p.Glu260=
NM_000015.3:c.780G= MANE Select NP_000006.2:p.Glu260=