Canonical Allele Identifier: CA2830536750

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55599338T>A , CM000666.2:g.55599338T>A	GRCh38
NC_000004.11:g.56465505T>A , CM000666.1:g.56465505T>A	GRCh37
NC_000004.10:g.56160262T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.490-157A>T MANE Select	ENSP00000264218.3:n.490-157A>T
ENST00000505262.5:c.409-157A>T	ENSP00000424246.1:n.409-157A>T
ENST00000507338.1:c.415-157A>T	ENSP00000422870.1:n.415-157A>T
ENST00000509371.1:n.254-157A>T
ENST00000511469.5:c.442-157A>T	ENSP00000422399.1:n.442-157A>T
ENST00000515325.5:n.482-157A>T
NM_001292045.1:c.442-157A>T	NP_001278974.1:n.442-157A>T
NM_001292046.1:c.415-157A>T	NP_001278975.1:n.415-157A>T
NM_006681.3:c.490-157A>T	NP_006672.1:n.490-157A>T
NR_120489.1:n.482-157A>T
XM_011534367.1:c.439-157A>T	XP_011532669.1:n.439-157A>T
XM_011534368.1:c.388-157A>T	XP_011532670.1:n.388-157A>T
XM_011534367.2:c.439-157A>T	XP_011532669.1:n.439-157A>T
XM_011534368.3:c.388-157A>T	XP_011532670.1:n.388-157A>T
NM_006681.4:c.490-157A>T MANE Select	NP_006672.1:n.490-157A>T
NM_001292045.2:c.442-157A>T	NP_001278974.1:n.442-157A>T
NM_001292046.2:c.415-157A>T	NP_001278975.1:n.415-157A>T
NR_120489.2:n.577-157A>T