Canonical Allele Identifier: CA2525004901
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393399_18393400insGAAAATA , CM000670.2:g.18393399_18393400insGAAAATA GRCh38
NC_000008.10:g.18250909_18250910insGAAAATA , CM000670.1:g.18250909_18250910insGAAAATA GRCh37
NC_000008.9:g.18295189_18295190insGAAAATA NCBI36
NG_012246.1:g.7155_7156insGAAAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-7+2054_-7+2055insGAAAATA MANE Select ENSP00000286479.3:n.-7+2054_-7+2055insGAAAATA
ENST00000286479.3:c.-7+2054_-7+2055insGAAAATA ENSP00000286479.3:n.-7+2054_-7+2055insGAAAATA
ENST00000520116.1:c.-58+2054_-58+2055insGAAAATA ENSP00000428416.1:n.-58+2054_-58+2055insGAAAATA
NM_000015.2:c.-7+2054_-7+2055insGAAAATA NP_000006.2:n.-7+2054_-7+2055insGAAAATA
XM_011544358.1:c.-7+663_-7+664insGAAAATA XP_011542660.1:n.-7+663_-7+664insGAAAATA
XM_017012938.1:c.-7+6363_-7+6364insGAAAATA XP_016868427.1:n.-7+6363_-7+6364insGAAAATA
NM_000015.3:c.-7+2054_-7+2055insGAAAATA MANE Select NP_000006.2:n.-7+2054_-7+2055insGAAAATA