Canonical Allele Identifier: CA370636495

Gene: NAT2

Linked Data

• MyVariant Identifiers: chr8:g.18258239A>T (hg19) ; chr8:g.18400729A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400729A>T , CM000670.2:g.18400729A>T	GRCh38
NC_000008.10:g.18258239A>T , CM000670.1:g.18258239A>T	GRCh37
NC_000008.9:g.18302519A>T	NCBI36
NG_012246.1:g.14485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.726A>T MANE Select	ENSP00000286479.3:p.Arg242Ser
ENST00000286479.3:c.726A>T	ENSP00000286479.3:p.Arg242Ser
ENST00000520116.1:c.336A>T	ENSP00000428416.1:p.Arg112Ser
NM_000015.2:c.726A>T	NP_000006.2:p.Arg242Ser
XM_011544358.1:c.726A>T	XP_011542660.1:p.Arg242Ser
XM_017012938.1:c.726A>T	XP_016868427.1:p.Arg242Ser
NM_000015.3:c.726A>T MANE Select	NP_000006.2:p.Arg242Ser