Canonical Allele Identifier: CA1768218803
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400096G= , CM000670.2:g.18400096G= GRCh38
NC_000008.10:g.18257606G= , CM000670.1:g.18257606G= GRCh37
NC_000008.9:g.18301886G= NCBI36
NG_012246.1:g.13852G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.93G= MANE Select ENSP00000286479.3:p.Gln31=
ENST00000286479.3:c.93G= ENSP00000286479.3:p.Gln31=
ENST00000520116.1:c.-57-241G= ENSP00000428416.1:n.-57-241G=
NM_000015.2:c.93G= NP_000006.2:p.Gln31=
XM_011544358.1:c.93G= XP_011542660.1:p.Gln31=
XM_017012938.1:c.93G= XP_016868427.1:p.Gln31=
NM_000015.3:c.93G= MANE Select NP_000006.2:p.Gln31=