Canonical Allele Identifier: CA370635039

Gene: NAT2

Linked Data

• gnomAD v4: 8-18400047-C-T
• MyVariant Identifiers: chr8:g.18257557C>T (hg19) ; chr8:g.18400047C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400047C>T , CM000670.2:g.18400047C>T	GRCh38
NC_000008.10:g.18257557C>T , CM000670.1:g.18257557C>T	GRCh37
NC_000008.9:g.18301837C>T	NCBI36
NG_012246.1:g.13803C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.44C>T MANE Select	ENSP00000286479.3:p.Ser15Phe
ENST00000286479.3:c.44C>T	ENSP00000286479.3:p.Ser15Phe
ENST00000520116.1:c.-57-290C>T	ENSP00000428416.1:n.-57-290C>T
NM_000015.2:c.44C>T	NP_000006.2:p.Ser15Phe
XM_011544358.1:c.44C>T	XP_011542660.1:p.Ser15Phe
XM_017012938.1:c.44C>T	XP_016868427.1:p.Ser15Phe
NM_000015.3:c.44C>T MANE Select	NP_000006.2:p.Ser15Phe