Canonical Allele Identifier: CA1768126141

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210107G= , CM000670.2:g.18210107G=	GRCh38
NC_000008.10:g.18067616G= , CM000670.1:g.18067616G=	GRCh37
NC_000008.9:g.18111896G=	NCBI36
NG_012245.2:g.44646G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.8:c.-159G=	ENSP00000307218.4:n.-159G=
ENST00000517441.5:n.267+152G=
NM_000662.7:c.-159G=	NP_000653.3:n.-159G=
NM_001160170.3:c.-693G=	NP_001153642.1:n.-693G=
NM_001160171.3:c.-543G=	NP_001153643.1:n.-543G=
NM_001160172.3:c.-464G=	NP_001153644.1:n.-464G=
NM_001160173.3:c.-309G=	NP_001153645.1:n.-309G=
NM_001160175.3:c.-241G=	NP_001153647.1:n.-241G=
NM_001160176.3:c.-91G=	NP_001153648.1:n.-91G=
NM_001160179.2:c.-86+152G=	NP_001153651.1:n.-86+152G=
NM_001291962.1:c.-18+152G=	NP_001278891.1:n.-18+152G=
XM_011544687.1:c.-625G=	XP_011542989.1:n.-625G=
XM_011544688.1:c.-475G=	XP_011542990.1:n.-475G=
XM_017013947.1:c.-552+152G=	XP_016869436.1:n.-552+152G=
NM_001160179.3:c.-86+152G=	NP_001153651.1:n.-86+152G=
NM_001291962.2:c.-18+152G=	NP_001278891.1:n.-18+152G=