Canonical Allele Identifier: CA173519896
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs879179577

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400193_18400194delinsT , CM000670.2:g.18400193_18400194delinsT GRCh38
NC_000008.10:g.18257703_18257704delinsT , CM000670.1:g.18257703_18257704delinsT GRCh37
NC_000008.9:g.18301983_18301984delinsT NCBI36
NG_012246.1:g.13949_13950delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.190_191delinsT MANE Select ENSP00000286479.3:p.Arg64TrpfsTer16
ENST00000286479.3:c.190_191delinsT ENSP00000286479.3:p.Arg64TrpfsTer16
ENST00000520116.1:c.-57-144_-57-143delinsT ENSP00000428416.1:n.-57-144_-57-143delins...
NM_000015.2:c.190_191delinsT NP_000006.2:p.Arg64TrpfsTer16
XM_011544358.1:c.190_191delinsT XP_011542660.1:p.Arg64TrpfsTer16
XM_017012938.1:c.190_191delinsT XP_016868427.1:p.Arg64TrpfsTer16
NM_000015.3:c.190_191delinsT MANE Select NP_000006.2:p.Arg64TrpfsTer16