Canonical Allele Identifier: CA1768126162

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210143A= , CM000670.2:g.18210143A=	GRCh38
NC_000008.10:g.18067652A= , CM000670.1:g.18067652A=	GRCh37
NC_000008.9:g.18111932A=	NCBI36
NG_012245.2:g.44682A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-123A= MANE Select	ENSP00000307218.4:n.-123A=
ENST00000307719.8:c.-123A=	ENSP00000307218.4:n.-123A=
ENST00000517441.5:n.267+188A=
ENST00000517574.5:n.10A=
ENST00000518029.5:c.-507A=	ENSP00000428270.1:n.-507A=
ENST00000541942.1:c.-273A=	ENSP00000440900.1:n.-273A=
NM_000662.7:c.-123A=	NP_000653.3:n.-123A=
NM_001160170.3:c.-657A=	NP_001153642.1:n.-657A=
NM_001160171.3:c.-507A=	NP_001153643.1:n.-507A=
NM_001160172.3:c.-428A=	NP_001153644.1:n.-428A=
NM_001160173.3:c.-273A=	NP_001153645.1:n.-273A=
NM_001160175.3:c.-205A=	NP_001153647.1:n.-205A=
NM_001160176.3:c.-55A=	NP_001153648.1:n.-55A=
NM_001160179.2:c.-86+188A=	NP_001153651.1:n.-86+188A=
NM_001291962.1:c.-18+188A=	NP_001278891.1:n.-18+188A=
XM_011544687.1:c.-589A=	XP_011542989.1:n.-589A=
XM_011544688.1:c.-439A=	XP_011542990.1:n.-439A=
XM_017013947.1:c.-552+188A=	XP_016869436.1:n.-552+188A=
NM_000662.8:c.-123A= MANE Select	NP_000653.3:n.-123A=
NM_001160170.4:c.-657A=	NP_001153642.1:n.-657A=
NM_001160171.4:c.-507A=	NP_001153643.1:n.-507A=
NM_001160172.4:c.-428A=	NP_001153644.1:n.-428A=
NM_001160175.4:c.-205A=	NP_001153647.1:n.-205A=
NM_001160176.4:c.-55A=	NP_001153648.1:n.-55A=
NM_001160179.3:c.-86+188A=	NP_001153651.1:n.-86+188A=
NM_001291962.2:c.-18+188A=	NP_001278891.1:n.-18+188A=
NM_001160173.4:c.-273A=	NP_001153645.1:n.-273A=