Canonical Allele Identifier: CA1768215495
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1800623025
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393444del , CM000670.2:g.18393444del GRCh38
NC_000008.10:g.18250954del , CM000670.1:g.18250954del GRCh37
NC_000008.9:g.18295234del NCBI36
NG_012246.1:g.7200del

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+2099del MANE Select ENSP00000286479.3:n.-7+2099del
ENST00000286479.3:c.-7+2099del ENSP00000286479.3:n.-7+2099del
ENST00000520116.1:c.-58+2099del ENSP00000428416.1:n.-58+2099del
NM_000015.2:c.-7+2099del NP_000006.2:n.-7+2099del
XM_011544358.1:c.-7+708del XP_011542660.1:n.-7+708del
XM_017012938.1:c.-7+6408del XP_016868427.1:n.-7+6408del
NM_000015.3:c.-7+2099del MANE Select NP_000006.2:n.-7+2099del
Search 100 bp 5'
Search 100 bp 3'