Canonical Allele Identifier: CA173519895
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs879179577

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400193_18400194delinsA , CM000670.2:g.18400193_18400194delinsA GRCh38
NC_000008.10:g.18257703_18257704delinsA , CM000670.1:g.18257703_18257704delinsA GRCh37
NC_000008.9:g.18301983_18301984delinsA NCBI36
NG_012246.1:g.13949_13950delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.190_191delinsA MANE Select ENSP00000286479.3:p.Gly65ValfsTer15
ENST00000286479.3:c.190_191delinsA ENSP00000286479.3:p.Gly65ValfsTer15
ENST00000520116.1:c.-57-144_-57-143delinsA ENSP00000428416.1:n.-57-144_-57-143delins...
NM_000015.2:c.190_191delinsA NP_000006.2:p.Gly65ValfsTer15
XM_011544358.1:c.190_191delinsA XP_011542660.1:p.Gly65ValfsTer15
XM_017012938.1:c.190_191delinsA XP_016868427.1:p.Gly65ValfsTer15
NM_000015.3:c.190_191delinsA MANE Select NP_000006.2:p.Gly65ValfsTer15