Canonical Allele Identifier: CA1768215432

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18393320_18393321delinsCT , CM000670.2:g.18393320_18393321delinsCT	GRCh38
NC_000008.10:g.18250830_18250831delinsCT , CM000670.1:g.18250830_18250831delinsCT	GRCh37
NC_000008.9:g.18295110_18295111delinsCT	NCBI36
NG_012246.1:g.7076_7077delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.-7+1975_-7+1976delinsCT MANE Select	ENSP00000286479.3:n.-7+1975_-7+1976delinsCT
ENST00000286479.3:c.-7+1975_-7+1976delinsCT	ENSP00000286479.3:n.-7+1975_-7+1976delinsCT
ENST00000520116.1:c.-58+1975_-58+1976delinsCT	ENSP00000428416.1:n.-58+1975_-58+1976delinsCT
NM_000015.2:c.-7+1975_-7+1976delinsCT	NP_000006.2:n.-7+1975_-7+1976delinsCT
XM_011544358.1:c.-7+584_-7+585delinsCT	XP_011542660.1:n.-7+584_-7+585delinsCT
XM_017012938.1:c.-7+6284_-7+6285delinsCT	XP_016868427.1:n.-7+6284_-7+6285delinsCT
NM_000015.3:c.-7+1975_-7+1976delinsCT MANE Select	NP_000006.2:n.-7+1975_-7+1976delinsCT