Canonical Allele Identifier: CA1768219209

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400893A= , CM000670.2:g.18400893A=	GRCh38
NC_000008.10:g.18258403A= , CM000670.1:g.18258403A=	GRCh37
NC_000008.9:g.18302683A=	NCBI36
NG_012246.1:g.14649A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.*17A= MANE Select	ENSP00000286479.3:n.*17A=
ENST00000286479.3:c.*17A=	ENSP00000286479.3:n.*17A=
ENST00000520116.1:c.*17A=	ENSP00000428416.1:n.*17A=
NM_000015.2:c.*17A=	NP_000006.2:n.*17A=
XM_011544358.1:c.*17A=	XP_011542660.1:n.*17A=
XM_017012938.1:c.*17A=	XP_016868427.1:n.*17A=
NM_000015.3:c.*17A= MANE Select	NP_000006.2:n.*17A=