Canonical Allele Identifier: CA1768126153

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210128A= , CM000670.2:g.18210128A=	GRCh38
NC_000008.10:g.18067637A= , CM000670.1:g.18067637A=	GRCh37
NC_000008.9:g.18111917A=	NCBI36
NG_012245.2:g.44667A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-138A= MANE Select	ENSP00000307218.4:n.-138A=
ENST00000307719.8:c.-138A=	ENSP00000307218.4:n.-138A=
ENST00000517441.5:n.267+173A=
ENST00000541942.1:c.-288A=	ENSP00000440900.1:n.-288A=
NM_000662.7:c.-138A=	NP_000653.3:n.-138A=
NM_001160170.3:c.-672A=	NP_001153642.1:n.-672A=
NM_001160171.3:c.-522A=	NP_001153643.1:n.-522A=
NM_001160172.3:c.-443A=	NP_001153644.1:n.-443A=
NM_001160173.3:c.-288A=	NP_001153645.1:n.-288A=
NM_001160175.3:c.-220A=	NP_001153647.1:n.-220A=
NM_001160176.3:c.-70A=	NP_001153648.1:n.-70A=
NM_001160179.2:c.-86+173A=	NP_001153651.1:n.-86+173A=
NM_001291962.1:c.-18+173A=	NP_001278891.1:n.-18+173A=
XM_011544687.1:c.-604A=	XP_011542989.1:n.-604A=
XM_011544688.1:c.-454A=	XP_011542990.1:n.-454A=
XM_017013947.1:c.-552+173A=	XP_016869436.1:n.-552+173A=
NM_000662.8:c.-138A= MANE Select	NP_000653.3:n.-138A=
NM_001160170.4:c.-672A=	NP_001153642.1:n.-672A=
NM_001160171.4:c.-522A=	NP_001153643.1:n.-522A=
NM_001160172.4:c.-443A=	NP_001153644.1:n.-443A=
NM_001160175.4:c.-220A=	NP_001153647.1:n.-220A=
NM_001160176.4:c.-70A=	NP_001153648.1:n.-70A=
NM_001160179.3:c.-86+173A=	NP_001153651.1:n.-86+173A=
NM_001291962.2:c.-18+173A=	NP_001278891.1:n.-18+173A=
NM_001160173.4:c.-288A=	NP_001153645.1:n.-288A=