Canonical Allele Identifier: CA8610637

Gene: NMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45098539G>A , CM000679.2:g.45098539G>A	GRCh38
NC_000017.10:g.43175907G>A , CM000679.1:g.43175907G>A	GRCh37
NC_000017.9:g.40531433G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258960.7:c.871G>A MANE Select	ENSP00000258960.2:p.Val291Ile
ENST00000587014.2:n.897G>A
ENST00000587670.2:c.*627G>A	ENSP00000504365.1:n.*627G>A
ENST00000590114.6:c.754G>A	ENSP00000504284.1:n.754G>A
ENST00000590310.2:c.871G>A	ENSP00000503657.1:p.Val291Ile
ENST00000591931.2:n.897G>A
ENST00000592654.3:c.631G>A	ENSP00000466827.2:p.Val211Ile
ENST00000676753.1:c.*945G>A	ENSP00000503505.1:n.*945G>A
ENST00000676828.1:c.871G>A	ENSP00000504192.1:p.Val291Ile
ENST00000677949.1:c.871G>A	ENSP00000504048.1:p.Val291Ile
ENST00000678332.1:c.*719G>A	ENSP00000504484.1:n.*719G>A
ENST00000678576.1:c.871G>A	ENSP00000503635.1:p.Val291Ile
ENST00000678606.1:n.897G>A
ENST00000678938.1:c.631G>A	ENSP00000503621.1:p.Val211Ile
ENST00000258960.6:c.871G>A	ENSP00000258960.2:p.Val291Ile
ENST00000543908.5:c.*338G>A	ENSP00000439263.1:n.*338G>A
ENST00000588455.5:n.540G>A
ENST00000590310.1:n.275G>A
ENST00000592782.5:c.871G>A	ENSP00000468424.1:p.Val291Ile
NM_021079.4:c.871G>A	NP_066565.1:p.Val291Ile
XM_011524858.1:c.871G>A	XP_011523160.1:p.Val291Ile
XR_002958013.1:n.881G>A
NM_021079.5:c.871G>A MANE Select	NP_066565.1:p.Val291Ile