Canonical Allele Identifier: CA1768218964
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400396G= , CM000670.2:g.18400396G= GRCh38
NC_000008.10:g.18257906G= , CM000670.1:g.18257906G= GRCh37
NC_000008.9:g.18302186G= NCBI36
NG_012246.1:g.14152G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.393G= MANE Select ENSP00000286479.3:p.Met131=
ENST00000286479.3:c.393G= ENSP00000286479.3:p.Met131=
ENST00000520116.1:c.3G= ENSP00000428416.1:p.Met1=
NM_000015.2:c.393G= NP_000006.2:p.Met131=
XM_011544358.1:c.393G= XP_011542660.1:p.Met131=
XM_017012938.1:c.393G= XP_016868427.1:p.Met131=
NM_000015.3:c.393G= MANE Select NP_000006.2:p.Met131=