Canonical Allele Identifier: CA173176758

Gene: NAT1

Linked Data

• dbSNP Id: rs759199114
• MyVariant Identifiers: chr8:g.18067637A>G (hg19) ; chr8:g.18210128A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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