Canonical Allele Identifier: CA370634999
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400027A>T , CM000670.2:g.18400027A>T GRCh38
NC_000008.10:g.18257537A>T , CM000670.1:g.18257537A>T GRCh37
NC_000008.9:g.18301817A>T NCBI36
NG_012246.1:g.13783A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.24A>T MANE Select ENSP00000286479.3:p.Glu8Asp
ENST00000286479.3:c.24A>T ENSP00000286479.3:p.Glu8Asp
ENST00000520116.1:c.-57-310A>T ENSP00000428416.1:n.-57-310A>T
NM_000015.2:c.24A>T NP_000006.2:p.Glu8Asp
XM_011544358.1:c.24A>T XP_011542660.1:p.Glu8Asp
XM_017012938.1:c.24A>T XP_016868427.1:p.Glu8Asp
NM_000015.3:c.24A>T MANE Select NP_000006.2:p.Glu8Asp