Canonical Allele Identifier: CA1768218766

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400011T= , CM000670.2:g.18400011T=	GRCh38
NC_000008.10:g.18257521T= , CM000670.1:g.18257521T=	GRCh37
NC_000008.9:g.18301801T=	NCBI36
NG_012246.1:g.13767T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.8T= MANE Select	ENSP00000286479.3:p.Ile3=
ENST00000286479.3:c.8T=	ENSP00000286479.3:p.Ile3=
ENST00000520116.1:c.-57-326T=	ENSP00000428416.1:n.-57-326T=
NM_000015.2:c.8T=	NP_000006.2:p.Ile3=
XM_011544358.1:c.8T=	XP_011542660.1:p.Ile3=
XM_017012938.1:c.8T=	XP_016868427.1:p.Ile3=
NM_000015.3:c.8T= MANE Select	NP_000006.2:p.Ile3=