Canonical Allele Identifier: CA1768126147

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210117A= , CM000670.2:g.18210117A=	GRCh38
NC_000008.10:g.18067626A= , CM000670.1:g.18067626A=	GRCh37
NC_000008.9:g.18111906A=	NCBI36
NG_012245.2:g.44656A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-149A= MANE Select	ENSP00000307218.4:n.-149A=
ENST00000307719.8:c.-149A=	ENSP00000307218.4:n.-149A=
ENST00000517441.5:n.267+162A=
ENST00000541942.1:c.-299A=	ENSP00000440900.1:n.-299A=
NM_000662.7:c.-149A=	NP_000653.3:n.-149A=
NM_001160170.3:c.-683A=	NP_001153642.1:n.-683A=
NM_001160171.3:c.-533A=	NP_001153643.1:n.-533A=
NM_001160172.3:c.-454A=	NP_001153644.1:n.-454A=
NM_001160173.3:c.-299A=	NP_001153645.1:n.-299A=
NM_001160175.3:c.-231A=	NP_001153647.1:n.-231A=
NM_001160176.3:c.-81A=	NP_001153648.1:n.-81A=
NM_001160179.2:c.-86+162A=	NP_001153651.1:n.-86+162A=
NM_001291962.1:c.-18+162A=	NP_001278891.1:n.-18+162A=
XM_011544687.1:c.-615A=	XP_011542989.1:n.-615A=
XM_011544688.1:c.-465A=	XP_011542990.1:n.-465A=
XM_017013947.1:c.-552+162A=	XP_016869436.1:n.-552+162A=
NM_000662.8:c.-149A= MANE Select	NP_000653.3:n.-149A=
NM_001160170.4:c.-683A=	NP_001153642.1:n.-683A=
NM_001160171.4:c.-533A=	NP_001153643.1:n.-533A=
NM_001160172.4:c.-454A=	NP_001153644.1:n.-454A=
NM_001160175.4:c.-231A=	NP_001153647.1:n.-231A=
NM_001160176.4:c.-81A=	NP_001153648.1:n.-81A=
NM_001160179.3:c.-86+162A=	NP_001153651.1:n.-86+162A=
NM_001291962.2:c.-18+162A=	NP_001278891.1:n.-18+162A=
NM_001160173.4:c.-299A=	NP_001153645.1:n.-299A=