Canonical Allele Identifier: CA1768218786
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400063C= , CM000670.2:g.18400063C= GRCh38
NC_000008.10:g.18257573C= , CM000670.1:g.18257573C= GRCh37
NC_000008.9:g.18301853C= NCBI36
NG_012246.1:g.13819C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.60C= MANE Select ENSP00000286479.3:p.Asp20=
ENST00000286479.3:c.60C= ENSP00000286479.3:p.Asp20=
ENST00000520116.1:c.-57-274C= ENSP00000428416.1:n.-57-274C=
NM_000015.2:c.60C= NP_000006.2:p.Asp20=
XM_011544358.1:c.60C= XP_011542660.1:p.Asp20=
XM_017012938.1:c.60C= XP_016868427.1:p.Asp20=
NM_000015.3:c.60C= MANE Select NP_000006.2:p.Asp20=