Canonical Allele Identifier: CA370635146
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400095A>C , CM000670.2:g.18400095A>C GRCh38
NC_000008.10:g.18257605A>C , CM000670.1:g.18257605A>C GRCh37
NC_000008.9:g.18301885A>C NCBI36
NG_012246.1:g.13851A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.92A>C MANE Select ENSP00000286479.3:p.Gln31Pro
ENST00000286479.3:c.92A>C ENSP00000286479.3:p.Gln31Pro
ENST00000520116.1:c.-57-242A>C ENSP00000428416.1:n.-57-242A>C
NM_000015.2:c.92A>C NP_000006.2:p.Gln31Pro
XM_011544358.1:c.92A>C XP_011542660.1:p.Gln31Pro
XM_017012938.1:c.92A>C XP_016868427.1:p.Gln31Pro
NM_000015.3:c.92A>C MANE Select NP_000006.2:p.Gln31Pro