Canonical Allele Identifier: CA1768218823
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400135_18400136delinsTG , CM000670.2:g.18400135_18400136delinsTG GRCh38
NC_000008.10:g.18257645_18257646delinsTG , CM000670.1:g.18257645_18257646delinsTG GRCh37
NC_000008.9:g.18301925_18301926delinsTG NCBI36
NG_012246.1:g.13891_13892delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.132_133delinsTG MANE Select ENSP00000286479.3:p.Cys44=
ENST00000286479.3:c.132_133delinsTG ENSP00000286479.3:p.Cys44=
ENST00000520116.1:c.-57-202_-57-201delinsTG ENSP00000428416.1:n.-57-202_-57-201delinsTG
NM_000015.2:c.132_133delinsTG NP_000006.2:p.Cys44=
XM_011544358.1:c.132_133delinsTG XP_011542660.1:p.Cys44=
XM_017012938.1:c.132_133delinsTG XP_016868427.1:p.Cys44=
NM_000015.3:c.132_133delinsTG MANE Select NP_000006.2:p.Cys44=