Canonical Allele Identifier: CA1768218910
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400290C= , CM000670.2:g.18400290C= GRCh38
NC_000008.10:g.18257800C= , CM000670.1:g.18257800C= GRCh37
NC_000008.9:g.18302080C= NCBI36
NG_012246.1:g.14046C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.287C= MANE Select ENSP00000286479.3:p.Pro96=
ENST00000286479.3:c.287C= ENSP00000286479.3:p.Pro96=
ENST00000520116.1:c.-57-47C= ENSP00000428416.1:n.-57-47C=
NM_000015.2:c.287C= NP_000006.2:p.Pro96=
XM_011544358.1:c.287C= XP_011542660.1:p.Pro96=
XM_017012938.1:c.287C= XP_016868427.1:p.Pro96=
NM_000015.3:c.287C= MANE Select NP_000006.2:p.Pro96=