Canonical Allele Identifier: CA1768126150

Gene: NAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210122C= , CM000670.2:g.18210122C=	GRCh38
NC_000008.10:g.18067631C= , CM000670.1:g.18067631C=	GRCh37
NC_000008.9:g.18111911C=	NCBI36
NG_012245.2:g.44661C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-144C= MANE Select	ENSP00000307218.4:n.-144C=
ENST00000307719.8:c.-144C=	ENSP00000307218.4:n.-144C=
ENST00000517441.5:n.267+167C=
ENST00000541942.1:c.-294C=	ENSP00000440900.1:n.-294C=
NM_000662.7:c.-144C=	NP_000653.3:n.-144C=
NM_001160170.3:c.-678C=	NP_001153642.1:n.-678C=
NM_001160171.3:c.-528C=	NP_001153643.1:n.-528C=
NM_001160172.3:c.-449C=	NP_001153644.1:n.-449C=
NM_001160173.3:c.-294C=	NP_001153645.1:n.-294C=
NM_001160175.3:c.-226C=	NP_001153647.1:n.-226C=
NM_001160176.3:c.-76C=	NP_001153648.1:n.-76C=
NM_001160179.2:c.-86+167C=	NP_001153651.1:n.-86+167C=
NM_001291962.1:c.-18+167C=	NP_001278891.1:n.-18+167C=
XM_011544687.1:c.-610C=	XP_011542989.1:n.-610C=
XM_011544688.1:c.-460C=	XP_011542990.1:n.-460C=
XM_017013947.1:c.-552+167C=	XP_016869436.1:n.-552+167C=
NM_000662.8:c.-144C= MANE Select	NP_000653.3:n.-144C=
NM_001160170.4:c.-678C=	NP_001153642.1:n.-678C=
NM_001160171.4:c.-528C=	NP_001153643.1:n.-528C=
NM_001160172.4:c.-449C=	NP_001153644.1:n.-449C=
NM_001160175.4:c.-226C=	NP_001153647.1:n.-226C=
NM_001160176.4:c.-76C=	NP_001153648.1:n.-76C=
NM_001160179.3:c.-86+167C=	NP_001153651.1:n.-86+167C=
NM_001291962.2:c.-18+167C=	NP_001278891.1:n.-18+167C=
NM_001160173.4:c.-294C=	NP_001153645.1:n.-294C=