Canonical Allele Identifier: CA459881164

Gene: NAT2

Linked Data

• MyVariant Identifiers: chr8:g.18258041T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400531T>A , CM000670.2:g.18400531T>A	GRCh38
NC_000008.10:g.18258041T>A , CM000670.1:g.18258041T>A	GRCh37
NC_000008.9:g.18302321T>A	NCBI36
NG_012246.1:g.14287T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.528T>A MANE Select	ENSP00000286479.3:p.Leu176=
ENST00000286479.3:c.528T>A	ENSP00000286479.3:p.Leu176=
ENST00000520116.1:c.138T>A	ENSP00000428416.1:p.Leu46=
NM_000015.2:c.528T>A	NP_000006.2:p.Leu176=
XM_011544358.1:c.528T>A	XP_011542660.1:p.Leu176=
XM_017012938.1:c.528T>A	XP_016868427.1:p.Leu176=
NM_000015.3:c.528T>A MANE Select	NP_000006.2:p.Leu176=