Canonical Allele Identifier: CA1768218925
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400319_18400320delinsGT , CM000670.2:g.18400319_18400320delinsGT GRCh38
NC_000008.10:g.18257829_18257830delinsGT , CM000670.1:g.18257829_18257830delinsGT GRCh37
NC_000008.9:g.18302109_18302110delinsGT NCBI36
NG_012246.1:g.14075_14076delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.316_317delinsGT MANE Select ENSP00000286479.3:p.Val106=
ENST00000286479.3:c.316_317delinsGT ENSP00000286479.3:p.Val106=
ENST00000520116.1:c.-57-18_-57-17delinsGT ENSP00000428416.1:n.-57-18_-57-17delinsGT
NM_000015.2:c.316_317delinsGT NP_000006.2:p.Val106=
XM_011544358.1:c.316_317delinsGT XP_011542660.1:p.Val106=
XM_017012938.1:c.316_317delinsGT XP_016868427.1:p.Val106=
NM_000015.3:c.316_317delinsGT MANE Select NP_000006.2:p.Val106=