Canonical Allele Identifier: CA2559983902

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18393402_18393403insAATGA , CM000670.2:g.18393402_18393403insAATGA	GRCh38
NC_000008.10:g.18250912_18250913insAATGA , CM000670.1:g.18250912_18250913insAATGA	GRCh37
NC_000008.9:g.18295192_18295193insAATGA	NCBI36
NG_012246.1:g.7158_7159insAATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.-7+2057_-7+2058insAATGA MANE Select	ENSP00000286479.3:n.-7+2057_-7+2058insAATGA
ENST00000286479.3:c.-7+2057_-7+2058insAATGA	ENSP00000286479.3:n.-7+2057_-7+2058insAATGA
ENST00000520116.1:c.-58+2057_-58+2058insAATGA	ENSP00000428416.1:n.-58+2057_-58+2058insAATGA
NM_000015.2:c.-7+2057_-7+2058insAATGA	NP_000006.2:n.-7+2057_-7+2058insAATGA
XM_011544358.1:c.-7+666_-7+667insAATGA	XP_011542660.1:n.-7+666_-7+667insAATGA
XM_017012938.1:c.-7+6366_-7+6367insAATGA	XP_016868427.1:n.-7+6366_-7+6367insAATGA
NM_000015.3:c.-7+2057_-7+2058insAATGA MANE Select	NP_000006.2:n.-7+2057_-7+2058insAATGA