Canonical Allele Identifier: CA2686326438
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400273_18400275del , CM000670.2:g.18400273_18400275del GRCh38
NC_000008.10:g.18257783_18257785del , CM000670.1:g.18257783_18257785del GRCh37
NC_000008.9:g.18302063_18302065del NCBI36
NG_012246.1:g.14029_14031del

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.270_272del MANE Select ENSP00000286479.3:p.Gly91del
ENST00000286479.3:c.270_272del ENSP00000286479.3:p.Gly91del
ENST00000520116.1:c.-57-64_-57-62del ENSP00000428416.1:n.-57-64_-57-62del
NM_000015.2:c.270_272del NP_000006.2:p.Gly91del
XM_011544358.1:c.270_272del XP_011542660.1:p.Gly91del
XM_017012938.1:c.270_272del XP_016868427.1:p.Gly91del
NM_000015.3:c.270_272del MANE Select NP_000006.2:p.Gly91del