Canonical Allele Identifier: CA1768126168

Gene: NAT1

Linked Data

• dbSNP Id: rs1190327365

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18210150C>T , CM000670.2:g.18210150C>T	GRCh38
NC_000008.10:g.18067659C>T , CM000670.1:g.18067659C>T	GRCh37
NC_000008.9:g.18111939C>T	NCBI36
NG_012245.2:g.44689C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307719.9:c.-116C>T MANE Select	ENSP00000307218.4:n.-116C>T
ENST00000307719.8:c.-116C>T	ENSP00000307218.4:n.-116C>T
ENST00000517441.5:n.267+195C>T
ENST00000517574.5:n.17C>T
ENST00000518029.5:c.-500C>T	ENSP00000428270.1:n.-500C>T
ENST00000541942.1:c.-266C>T	ENSP00000440900.1:n.-266C>T
NM_000662.7:c.-116C>T	NP_000653.3:n.-116C>T
NM_001160170.3:c.-650C>T	NP_001153642.1:n.-650C>T
NM_001160171.3:c.-500C>T	NP_001153643.1:n.-500C>T
NM_001160172.3:c.-421C>T	NP_001153644.1:n.-421C>T
NM_001160173.3:c.-266C>T	NP_001153645.1:n.-266C>T
NM_001160175.3:c.-198C>T	NP_001153647.1:n.-198C>T
NM_001160176.3:c.-48C>T	NP_001153648.1:n.-48C>T
NM_001160179.2:c.-86+195C>T	NP_001153651.1:n.-86+195C>T
NM_001291962.1:c.-18+195C>T	NP_001278891.1:n.-18+195C>T
XM_011544687.1:c.-582C>T	XP_011542989.1:n.-582C>T
XM_011544688.1:c.-432C>T	XP_011542990.1:n.-432C>T
XM_017013947.1:c.-552+195C>T	XP_016869436.1:n.-552+195C>T
NM_000662.8:c.-116C>T MANE Select	NP_000653.3:n.-116C>T
NM_001160170.4:c.-650C>T	NP_001153642.1:n.-650C>T
NM_001160171.4:c.-500C>T	NP_001153643.1:n.-500C>T
NM_001160172.4:c.-421C>T	NP_001153644.1:n.-421C>T
NM_001160175.4:c.-198C>T	NP_001153647.1:n.-198C>T
NM_001160176.4:c.-48C>T	NP_001153648.1:n.-48C>T
NM_001160179.3:c.-86+195C>T	NP_001153651.1:n.-86+195C>T
NM_001291962.2:c.-18+195C>T	NP_001278891.1:n.-18+195C>T
NM_001160173.4:c.-266C>T	NP_001153645.1:n.-266C>T