Canonical Allele Identifier: CA1768218837
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400157T= , CM000670.2:g.18400157T= GRCh38
NC_000008.10:g.18257667T= , CM000670.1:g.18257667T= GRCh37
NC_000008.9:g.18301947T= NCBI36
NG_012246.1:g.13913T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.154T= MANE Select ENSP00000286479.3:p.Leu52=
ENST00000286479.3:c.154T= ENSP00000286479.3:p.Leu52=
ENST00000520116.1:c.-57-180T= ENSP00000428416.1:n.-57-180T=
NM_000015.2:c.154T= NP_000006.2:p.Leu52=
XM_011544358.1:c.154T= XP_011542660.1:p.Leu52=
XM_017012938.1:c.154T= XP_016868427.1:p.Leu52=
NM_000015.3:c.154T= MANE Select NP_000006.2:p.Leu52=