Canonical Allele Identifier: CA1768219224
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400919C= , CM000670.2:g.18400919C= GRCh38
NC_000008.10:g.18258429C= , CM000670.1:g.18258429C= GRCh37
NC_000008.9:g.18302709C= NCBI36
NG_012246.1:g.14675C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.*43C= MANE Select ENSP00000286479.3:n.*43C=
ENST00000286479.3:c.*43C= ENSP00000286479.3:n.*43C=
ENST00000520116.1:c.*43C= ENSP00000428416.1:n.*43C=
NM_000015.2:c.*43C= NP_000006.2:n.*43C=
XM_011544358.1:c.*43C= XP_011542660.1:n.*43C=
XM_017012938.1:c.*43C= XP_016868427.1:n.*43C=
NM_000015.3:c.*43C= MANE Select NP_000006.2:n.*43C=