Canonical Allele Identifier: CA2522744224

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55600967_55600968del , CM000666.2:g.55600967_55600968del	GRCh38
NC_000004.11:g.56467134_56467135del , CM000666.1:g.56467134_56467135del	GRCh37
NC_000004.10:g.56161891_56161892del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.436-393_436-392del MANE Select	ENSP00000264218.3:n.436-393_436-392del
ENST00000505262.5:c.355-393_355-392del	ENSP00000424246.1:n.355-393_355-392del
ENST00000507338.1:c.361-393_361-392del	ENSP00000422870.1:n.361-393_361-392del
ENST00000509371.1:n.200-393_200-392del
ENST00000511469.5:c.388-393_388-392del	ENSP00000422399.1:n.388-393_388-392del
ENST00000515325.5:n.428-393_428-392del
NM_001292045.1:c.388-393_388-392del	NP_001278974.1:n.388-393_388-392del
NM_001292046.1:c.361-393_361-392del	NP_001278975.1:n.361-393_361-392del
NM_006681.3:c.436-393_436-392del	NP_006672.1:n.436-393_436-392del
NR_120489.1:n.428-393_428-392del
XM_011534367.1:c.385-393_385-392del	XP_011532669.1:n.385-393_385-392del
XM_011534368.1:c.334-393_334-392del	XP_011532670.1:n.334-393_334-392del
XM_011534367.2:c.385-393_385-392del	XP_011532669.1:n.385-393_385-392del
XM_011534368.3:c.334-393_334-392del	XP_011532670.1:n.334-393_334-392del
NM_006681.4:c.436-393_436-392del MANE Select	NP_006672.1:n.436-393_436-392del
NM_001292045.2:c.388-393_388-392del	NP_001278974.1:n.388-393_388-392del
NM_001292046.2:c.361-393_361-392del	NP_001278975.1:n.361-393_361-392del
NR_120489.2:n.523-393_523-392del