Canonical Allele Identifier: CA1768218965

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400397T= , CM000670.2:g.18400397T=	GRCh38
NC_000008.10:g.18257907T= , CM000670.1:g.18257907T=	GRCh37
NC_000008.9:g.18302187T=	NCBI36
NG_012246.1:g.14153T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.394T= MANE Select	ENSP00000286479.3:p.Trp132=
ENST00000286479.3:c.394T=	ENSP00000286479.3:p.Trp132=
ENST00000520116.1:c.4T=	ENSP00000428416.1:p.Trp2=
NM_000015.2:c.394T=	NP_000006.2:p.Trp132=
XM_011544358.1:c.394T=	XP_011542660.1:p.Trp132=
XM_017012938.1:c.394T=	XP_016868427.1:p.Trp132=
NM_000015.3:c.394T= MANE Select	NP_000006.2:p.Trp132=