Canonical Allele Identifier: CA370636787
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400869C>A , CM000670.2:g.18400869C>A GRCh38
NC_000008.10:g.18258379C>A , CM000670.1:g.18258379C>A GRCh37
NC_000008.9:g.18302659C>A NCBI36
NG_012246.1:g.14625C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.866C>A MANE Select ENSP00000286479.3:p.Thr289Asn
ENST00000286479.3:c.866C>A ENSP00000286479.3:p.Thr289Asn
ENST00000520116.1:c.476C>A ENSP00000428416.1:p.Thr159Asn
NM_000015.2:c.866C>A NP_000006.2:p.Thr289Asn
XM_011544358.1:c.866C>A XP_011542660.1:p.Thr289Asn
XM_017012938.1:c.866C>A XP_016868427.1:p.Thr289Asn
NM_000015.3:c.866C>A MANE Select NP_000006.2:p.Thr289Asn