Canonical Allele Identifier: CA1768218885
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400247A= , CM000670.2:g.18400247A= GRCh38
NC_000008.10:g.18257757A= , CM000670.1:g.18257757A= GRCh37
NC_000008.9:g.18302037A= NCBI36
NG_012246.1:g.14003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.244A= MANE Select ENSP00000286479.3:p.Ile82=
ENST00000286479.3:c.244A= ENSP00000286479.3:p.Ile82=
ENST00000520116.1:c.-57-90A= ENSP00000428416.1:n.-57-90A=
NM_000015.2:c.244A= NP_000006.2:p.Ile82=
XM_011544358.1:c.244A= XP_011542660.1:p.Ile82=
XM_017012938.1:c.244A= XP_016868427.1:p.Ile82=
NM_000015.3:c.244A= MANE Select NP_000006.2:p.Ile82=