Canonical Allele Identifier: CA1459162455
Gene: NMU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55601088G= , CM000666.2:g.55601088G= GRCh38
NC_000004.11:g.56467255G= , CM000666.1:g.56467255G= GRCh37
NC_000004.10:g.56162012G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264218.7:c.436-513C= MANE Select ENSP00000264218.3:n.436-513C=
ENST00000505262.5:c.355-513C= ENSP00000424246.1:n.355-513C=
ENST00000507338.1:c.361-513C= ENSP00000422870.1:n.361-513C=
ENST00000509371.1:n.200-513C=
ENST00000511469.5:c.388-513C= ENSP00000422399.1:n.388-513C=
ENST00000515325.5:n.428-513C=
NM_001292045.1:c.388-513C= NP_001278974.1:n.388-513C=
NM_001292046.1:c.361-513C= NP_001278975.1:n.361-513C=
NM_006681.3:c.436-513C= NP_006672.1:n.436-513C=
NR_120489.1:n.428-513C=
XM_011534367.1:c.385-513C= XP_011532669.1:n.385-513C=
XM_011534368.1:c.334-513C= XP_011532670.1:n.334-513C=
XM_011534367.2:c.385-513C= XP_011532669.1:n.385-513C=
XM_011534368.3:c.334-513C= XP_011532670.1:n.334-513C=
NM_006681.4:c.436-513C= MANE Select NP_006672.1:n.436-513C=
NM_001292045.2:c.388-513C= NP_001278974.1:n.388-513C=
NM_001292046.2:c.361-513C= NP_001278975.1:n.361-513C=
NR_120489.2:n.523-513C=