Canonical Allele Identifier: CA1768218978

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400430C= , CM000670.2:g.18400430C=	GRCh38
NC_000008.10:g.18257940C= , CM000670.1:g.18257940C=	GRCh37
NC_000008.9:g.18302220C=	NCBI36
NG_012246.1:g.14186C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.427C= MANE Select	ENSP00000286479.3:p.Gln143=
ENST00000286479.3:c.427C=	ENSP00000286479.3:p.Gln143=
ENST00000520116.1:c.37C=	ENSP00000428416.1:p.Gln13=
NM_000015.2:c.427C=	NP_000006.2:p.Gln143=
XM_011544358.1:c.427C=	XP_011542660.1:p.Gln143=
XM_017012938.1:c.427C=	XP_016868427.1:p.Gln143=
NM_000015.3:c.427C= MANE Select	NP_000006.2:p.Gln143=