Canonical Allele Identifier: CA1768219177
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400841G= , CM000670.2:g.18400841G= GRCh38
NC_000008.10:g.18258351G= , CM000670.1:g.18258351G= GRCh37
NC_000008.9:g.18302631G= NCBI36
NG_012246.1:g.14597G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.838G= MANE Select ENSP00000286479.3:p.Val280=
ENST00000286479.3:c.838G= ENSP00000286479.3:p.Val280=
ENST00000520116.1:c.448G= ENSP00000428416.1:p.Val150=
NM_000015.2:c.838G= NP_000006.2:p.Val280=
XM_011544358.1:c.838G= XP_011542660.1:p.Val280=
XM_017012938.1:c.838G= XP_016868427.1:p.Val280=
NM_000015.3:c.838G= MANE Select NP_000006.2:p.Val280=