Canonical Allele Identifier: CA1768126205

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210222T= , CM000670.2:g.18210222T=	GRCh38
NC_000008.10:g.18067731T= , CM000670.1:g.18067731T=	GRCh37
NC_000008.9:g.18112011T=	NCBI36
NG_012245.2:g.44761T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-86+42T= MANE Select	ENSP00000307218.4:n.-86+42T=
ENST00000307719.8:c.-86+42T=	ENSP00000307218.4:n.-86+42T=
ENST00000517441.5:n.267+267T=
ENST00000517574.5:n.47+42T=
ENST00000518029.5:c.-470+42T=	ENSP00000428270.1:n.-470+42T=
ENST00000541942.1:c.-236+42T=	ENSP00000440900.1:n.-236+42T=
NM_000662.7:c.-86+42T=	NP_000653.3:n.-86+42T=
NM_001160170.3:c.-620+42T=	NP_001153642.1:n.-620+42T=
NM_001160171.3:c.-470+42T=	NP_001153643.1:n.-470+42T=
NM_001160172.3:c.-391+42T=	NP_001153644.1:n.-391+42T=
NM_001160173.3:c.-236+42T=	NP_001153645.1:n.-236+42T=
NM_001160175.3:c.-168+42T=	NP_001153647.1:n.-168+42T=
NM_001160176.3:c.-18+42T=	NP_001153648.1:n.-18+42T=
NM_001160179.2:c.-86+267T=	NP_001153651.1:n.-86+267T=
NM_001291962.1:c.-18+267T=	NP_001278891.1:n.-18+267T=
XM_011544687.1:c.-552+42T=	XP_011542989.1:n.-552+42T=
XM_011544688.1:c.-402+42T=	XP_011542990.1:n.-402+42T=
XM_017013947.1:c.-552+267T=	XP_016869436.1:n.-552+267T=
NM_000662.8:c.-86+42T= MANE Select	NP_000653.3:n.-86+42T=
NM_001160170.4:c.-620+42T=	NP_001153642.1:n.-620+42T=
NM_001160171.4:c.-470+42T=	NP_001153643.1:n.-470+42T=
NM_001160172.4:c.-391+42T=	NP_001153644.1:n.-391+42T=
NM_001160175.4:c.-168+42T=	NP_001153647.1:n.-168+42T=
NM_001160176.4:c.-18+42T=	NP_001153648.1:n.-18+42T=
NM_001160179.3:c.-86+267T=	NP_001153651.1:n.-86+267T=
NM_001291962.2:c.-18+267T=	NP_001278891.1:n.-18+267T=
NM_001160173.4:c.-236+42T=	NP_001153645.1:n.-236+42T=