Canonical Allele Identifier: CA1768219181

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400848A= , CM000670.2:g.18400848A=	GRCh38
NC_000008.10:g.18258358A= , CM000670.1:g.18258358A=	GRCh37
NC_000008.9:g.18302638A=	NCBI36
NG_012246.1:g.14604A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.845A= MANE Select	ENSP00000286479.3:p.Lys282=
ENST00000286479.3:c.845A=	ENSP00000286479.3:p.Lys282=
ENST00000520116.1:c.455A=	ENSP00000428416.1:p.Lys152=
NM_000015.2:c.845A=	NP_000006.2:p.Lys282=
XM_011544358.1:c.845A=	XP_011542660.1:p.Lys282=
XM_017012938.1:c.845A=	XP_016868427.1:p.Lys282=
NM_000015.3:c.845A= MANE Select	NP_000006.2:p.Lys282=