Canonical Allele Identifier: CA1768219031
Community Standard Title: NM_000015.3(NAT2):c.540_542del (p.Leu181del)
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400543_18400545del , CM000670.2:g.18400543_18400545del GRCh38
NC_000008.10:g.18258053_18258055del , CM000670.1:g.18258053_18258055del GRCh37
NC_000008.9:g.18302333_18302335del NCBI36
NG_012246.1:g.14299_14301del

Transcript Alleles

HGVS Amino-acid Change
NM_000015.3:c.540_542del MANE Select NP_000006.2:p.Leu181del
ENST00000286479.4:c.540_542del MANE Select ENSP00000286479.3:p.Leu181del
NM_000015.2:c.540_542del NP_000006.2:p.Leu181del
ENST00000286479.3:c.540_542del ENSP00000286479.3:p.Leu181del
ENST00000520116.1:c.150_152del ENSP00000428416.1:p.Leu51del
XM_011544358.1:c.540_542del XP_011542660.1:p.Leu181del
XM_017012938.1:c.540_542del XP_016868427.1:p.Leu181del