Canonical Allele Identifier: CA1459162478

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55601154G= , CM000666.2:g.55601154G=	GRCh38
NC_000004.11:g.56467321G= , CM000666.1:g.56467321G=	GRCh37
NC_000004.10:g.56162078G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.436-579C= MANE Select	ENSP00000264218.3:n.436-579C=
ENST00000505262.5:c.355-579C=	ENSP00000424246.1:n.355-579C=
ENST00000507338.1:c.361-579C=	ENSP00000422870.1:n.361-579C=
ENST00000509371.1:n.200-579C=
ENST00000511469.5:c.388-579C=	ENSP00000422399.1:n.388-579C=
ENST00000515325.5:n.428-579C=
NM_001292045.1:c.388-579C=	NP_001278974.1:n.388-579C=
NM_001292046.1:c.361-579C=	NP_001278975.1:n.361-579C=
NM_006681.3:c.436-579C=	NP_006672.1:n.436-579C=
NR_120489.1:n.428-579C=
XM_011534367.1:c.385-579C=	XP_011532669.1:n.385-579C=
XM_011534368.1:c.334-579C=	XP_011532670.1:n.334-579C=
XM_011534367.2:c.385-579C=	XP_011532669.1:n.385-579C=
XM_011534368.3:c.334-579C=	XP_011532670.1:n.334-579C=
NM_006681.4:c.436-579C= MANE Select	NP_006672.1:n.436-579C=
NM_001292045.2:c.388-579C=	NP_001278974.1:n.388-579C=
NM_001292046.2:c.361-579C=	NP_001278975.1:n.361-579C=
NR_120489.2:n.523-579C=