Canonical Allele Identifier: CA1768215557

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18393575_18393576delinsAG , CM000670.2:g.18393575_18393576delinsAG	GRCh38
NC_000008.10:g.18251085_18251086delinsAG , CM000670.1:g.18251085_18251086delinsAG	GRCh37
NC_000008.9:g.18295365_18295366delinsAG	NCBI36
NG_012246.1:g.7331_7332delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.-7+2230_-7+2231delinsAG MANE Select	ENSP00000286479.3:n.-7+2230_-7+2231delinsAG
ENST00000286479.3:c.-7+2230_-7+2231delinsAG	ENSP00000286479.3:n.-7+2230_-7+2231delinsAG
ENST00000520116.1:c.-58+2230_-58+2231delinsAG	ENSP00000428416.1:n.-58+2230_-58+2231delinsAG
NM_000015.2:c.-7+2230_-7+2231delinsAG	NP_000006.2:n.-7+2230_-7+2231delinsAG
XM_011544358.1:c.-7+839_-7+840delinsAG	XP_011542660.1:n.-7+839_-7+840delinsAG
XM_017012938.1:c.-6-6423_-6-6422delinsAG	XP_016868427.1:n.-6-6423_-6-6422delinsAG
NM_000015.3:c.-7+2230_-7+2231delinsAG MANE Select	NP_000006.2:n.-7+2230_-7+2231delinsAG