Canonical Allele Identifier: CA2830536758

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55607546del , CM000666.2:g.55607546del	GRCh38
NC_000004.11:g.56473713del , CM000666.1:g.56473713del	GRCh37
NC_000004.10:g.56168470del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.280-80del MANE Select	ENSP00000264218.3:n.280-80del
ENST00000505262.5:c.279+1574del	ENSP00000424246.1:n.279+1574del
ENST00000507338.1:c.280-80del	ENSP00000422870.1:n.280-80del
ENST00000509371.1:n.170-80del
ENST00000511469.5:c.232-80del	ENSP00000422399.1:n.232-80del
ENST00000515325.5:n.323-80del
NM_001292045.1:c.232-80del	NP_001278974.1:n.232-80del
NM_001292046.1:c.280-80del	NP_001278975.1:n.280-80del
NM_006681.3:c.280-80del	NP_006672.1:n.280-80del
NR_120489.1:n.323-80del
XM_011534367.1:c.229-80del	XP_011532669.1:n.229-80del
XM_011534368.1:c.178-80del	XP_011532670.1:n.178-80del
XM_011534367.2:c.229-80del	XP_011532669.1:n.229-80del
XM_011534368.3:c.178-80del	XP_011532670.1:n.178-80del
NM_006681.4:c.280-80del MANE Select	NP_006672.1:n.280-80del
NM_001292045.2:c.232-80del	NP_001278974.1:n.232-80del
NM_001292046.2:c.280-80del	NP_001278975.1:n.280-80del
NR_120489.2:n.418-80del