Canonical Allele Identifier: CA1768126158

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210138A= , CM000670.2:g.18210138A=	GRCh38
NC_000008.10:g.18067647A= , CM000670.1:g.18067647A=	GRCh37
NC_000008.9:g.18111927A=	NCBI36
NG_012245.2:g.44677A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-128A= MANE Select	ENSP00000307218.4:n.-128A=
ENST00000307719.8:c.-128A=	ENSP00000307218.4:n.-128A=
ENST00000517441.5:n.267+183A=
ENST00000517574.5:n.5A=
ENST00000518029.5:c.-512A=	ENSP00000428270.1:n.-512A=
ENST00000541942.1:c.-278A=	ENSP00000440900.1:n.-278A=
NM_000662.7:c.-128A=	NP_000653.3:n.-128A=
NM_001160170.3:c.-662A=	NP_001153642.1:n.-662A=
NM_001160171.3:c.-512A=	NP_001153643.1:n.-512A=
NM_001160172.3:c.-433A=	NP_001153644.1:n.-433A=
NM_001160173.3:c.-278A=	NP_001153645.1:n.-278A=
NM_001160175.3:c.-210A=	NP_001153647.1:n.-210A=
NM_001160176.3:c.-60A=	NP_001153648.1:n.-60A=
NM_001160179.2:c.-86+183A=	NP_001153651.1:n.-86+183A=
NM_001291962.1:c.-18+183A=	NP_001278891.1:n.-18+183A=
XM_011544687.1:c.-594A=	XP_011542989.1:n.-594A=
XM_011544688.1:c.-444A=	XP_011542990.1:n.-444A=
XM_017013947.1:c.-552+183A=	XP_016869436.1:n.-552+183A=
NM_000662.8:c.-128A= MANE Select	NP_000653.3:n.-128A=
NM_001160170.4:c.-662A=	NP_001153642.1:n.-662A=
NM_001160171.4:c.-512A=	NP_001153643.1:n.-512A=
NM_001160172.4:c.-433A=	NP_001153644.1:n.-433A=
NM_001160175.4:c.-210A=	NP_001153647.1:n.-210A=
NM_001160176.4:c.-60A=	NP_001153648.1:n.-60A=
NM_001160179.3:c.-86+183A=	NP_001153651.1:n.-86+183A=
NM_001291962.2:c.-18+183A=	NP_001278891.1:n.-18+183A=
NM_001160173.4:c.-278A=	NP_001153645.1:n.-278A=