Canonical Allele Identifier: CA1768218815
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400122T= , CM000670.2:g.18400122T= GRCh38
NC_000008.10:g.18257632T= , CM000670.1:g.18257632T= GRCh37
NC_000008.9:g.18301912T= NCBI36
NG_012246.1:g.13878T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.119T= MANE Select ENSP00000286479.3:p.Leu40=
ENST00000286479.3:c.119T= ENSP00000286479.3:p.Leu40=
ENST00000520116.1:c.-57-215T= ENSP00000428416.1:n.-57-215T=
NM_000015.2:c.119T= NP_000006.2:p.Leu40=
XM_011544358.1:c.119T= XP_011542660.1:p.Leu40=
XM_017012938.1:c.119T= XP_016868427.1:p.Leu40=
NM_000015.3:c.119T= MANE Select NP_000006.2:p.Leu40=