Canonical Allele Identifier: CA1768219222

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400915A= , CM000670.2:g.18400915A=	GRCh38
NC_000008.10:g.18258425A= , CM000670.1:g.18258425A=	GRCh37
NC_000008.9:g.18302705A=	NCBI36
NG_012246.1:g.14671A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.*39A= MANE Select	ENSP00000286479.3:n.*39A=
ENST00000286479.3:c.*39A=	ENSP00000286479.3:n.*39A=
ENST00000520116.1:c.*39A=	ENSP00000428416.1:n.*39A=
NM_000015.2:c.*39A=	NP_000006.2:n.*39A=
XM_011544358.1:c.*39A=	XP_011542660.1:n.*39A=
XM_017012938.1:c.*39A=	XP_016868427.1:n.*39A=
NM_000015.3:c.*39A= MANE Select	NP_000006.2:n.*39A=