Canonical Allele Identifier: CA1768219079

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400636G= , CM000670.2:g.18400636G=	GRCh38
NC_000008.10:g.18258146G= , CM000670.1:g.18258146G=	GRCh37
NC_000008.9:g.18302426G=	NCBI36
NG_012246.1:g.14392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.633G= MANE Select	ENSP00000286479.3:p.Thr211=
ENST00000286479.3:c.633G=	ENSP00000286479.3:p.Thr211=
ENST00000520116.1:c.243G=	ENSP00000428416.1:p.Thr81=
NM_000015.2:c.633G=	NP_000006.2:p.Thr211=
XM_011544358.1:c.633G=	XP_011542660.1:p.Thr211=
XM_017012938.1:c.633G=	XP_016868427.1:p.Thr211=
NM_000015.3:c.633G= MANE Select	NP_000006.2:p.Thr211=