Canonical Allele Identifier: CA370635242
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400142G>A , CM000670.2:g.18400142G>A GRCh38
NC_000008.10:g.18257652G>A , CM000670.1:g.18257652G>A GRCh37
NC_000008.9:g.18301932G>A NCBI36
NG_012246.1:g.13898G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.139G>A MANE Select ENSP00000286479.3:p.Ala47Thr
ENST00000286479.3:c.139G>A ENSP00000286479.3:p.Ala47Thr
ENST00000520116.1:c.-57-195G>A ENSP00000428416.1:n.-57-195G>A
NM_000015.2:c.139G>A NP_000006.2:p.Ala47Thr
XM_011544358.1:c.139G>A XP_011542660.1:p.Ala47Thr
XM_017012938.1:c.139G>A XP_016868427.1:p.Ala47Thr
NM_000015.3:c.139G>A MANE Select NP_000006.2:p.Ala47Thr