Canonical Allele Identifier: CA370636413
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400689A>C , CM000670.2:g.18400689A>C GRCh38
NC_000008.10:g.18258199A>C , CM000670.1:g.18258199A>C GRCh37
NC_000008.9:g.18302479A>C NCBI36
NG_012246.1:g.14445A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.686A>C MANE Select ENSP00000286479.3:p.Glu229Ala
ENST00000286479.3:c.686A>C ENSP00000286479.3:p.Glu229Ala
ENST00000520116.1:c.296A>C ENSP00000428416.1:p.Glu99Ala
NM_000015.2:c.686A>C NP_000006.2:p.Glu229Ala
XM_011544358.1:c.686A>C XP_011542660.1:p.Glu229Ala
XM_017012938.1:c.686A>C XP_016868427.1:p.Glu229Ala
NM_000015.3:c.686A>C MANE Select NP_000006.2:p.Glu229Ala