Canonical Allele Identifier: CA1768218865
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400210C= , CM000670.2:g.18400210C= GRCh38
NC_000008.10:g.18257720C= , CM000670.1:g.18257720C= GRCh37
NC_000008.9:g.18302000C= NCBI36
NG_012246.1:g.13966C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.207C= MANE Select ENSP00000286479.3:p.Leu69=
ENST00000286479.3:c.207C= ENSP00000286479.3:p.Leu69=
ENST00000520116.1:c.-57-127C= ENSP00000428416.1:n.-57-127C=
NM_000015.2:c.207C= NP_000006.2:p.Leu69=
XM_011544358.1:c.207C= XP_011542660.1:p.Leu69=
XM_017012938.1:c.207C= XP_016868427.1:p.Leu69=
NM_000015.3:c.207C= MANE Select NP_000006.2:p.Leu69=