Canonical Allele Identifier: CA1768215494
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393443_18393444delinsTA , CM000670.2:g.18393443_18393444delinsTA GRCh38
NC_000008.10:g.18250953_18250954delinsTA , CM000670.1:g.18250953_18250954delinsTA GRCh37
NC_000008.9:g.18295233_18295234delinsTA NCBI36
NG_012246.1:g.7199_7200delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+2098_-7+2099delinsTA MANE Select ENSP00000286479.3:n.-7+2098_-7+2099delins...
ENST00000286479.3:c.-7+2098_-7+2099delinsTA ENSP00000286479.3:n.-7+2098_-7+2099delins...
ENST00000520116.1:c.-58+2098_-58+2099delinsTA ENSP00000428416.1:n.-58+2098_-58+2099deli...
NM_000015.2:c.-7+2098_-7+2099delinsTA NP_000006.2:n.-7+2098_-7+2099delinsTA
XM_011544358.1:c.-7+707_-7+708delinsTA XP_011542660.1:n.-7+707_-7+708delinsTA
XM_017012938.1:c.-7+6407_-7+6408delinsTA XP_016868427.1:n.-7+6407_-7+6408delinsTA
NM_000015.3:c.-7+2098_-7+2099delinsTA MANE Select NP_000006.2:n.-7+2098_-7+2099delinsTA