Canonical Allele Identifier: CA1459162511

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55601248_55601249delinsTA , CM000666.2:g.55601248_55601249delinsTA	GRCh38
NC_000004.11:g.56467415_56467416delinsTA , CM000666.1:g.56467415_56467416delinsTA	GRCh37
NC_000004.10:g.56162172_56162173delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.436-674_436-673delinsTA MANE Select	ENSP00000264218.3:n.436-674_436-673delinsTA
ENST00000505262.5:c.355-674_355-673delinsTA	ENSP00000424246.1:n.355-674_355-673delinsTA
ENST00000507338.1:c.361-674_361-673delinsTA	ENSP00000422870.1:n.361-674_361-673delinsTA
ENST00000509371.1:n.200-674_200-673delinsTA
ENST00000511469.5:c.388-674_388-673delinsTA	ENSP00000422399.1:n.388-674_388-673delinsTA
ENST00000515325.5:n.428-674_428-673delinsTA
NM_001292045.1:c.388-674_388-673delinsTA	NP_001278974.1:n.388-674_388-673delinsTA
NM_001292046.1:c.361-674_361-673delinsTA	NP_001278975.1:n.361-674_361-673delinsTA
NM_006681.3:c.436-674_436-673delinsTA	NP_006672.1:n.436-674_436-673delinsTA
NR_120489.1:n.428-674_428-673delinsTA
XM_011534367.1:c.385-674_385-673delinsTA	XP_011532669.1:n.385-674_385-673delinsTA
XM_011534368.1:c.334-674_334-673delinsTA	XP_011532670.1:n.334-674_334-673delinsTA
XM_011534367.2:c.385-674_385-673delinsTA	XP_011532669.1:n.385-674_385-673delinsTA
XM_011534368.3:c.334-674_334-673delinsTA	XP_011532670.1:n.334-674_334-673delinsTA
NM_006681.4:c.436-674_436-673delinsTA MANE Select	NP_006672.1:n.436-674_436-673delinsTA
NM_001292045.2:c.388-674_388-673delinsTA	NP_001278974.1:n.388-674_388-673delinsTA
NM_001292046.2:c.361-674_361-673delinsTA	NP_001278975.1:n.361-674_361-673delinsTA
NR_120489.2:n.523-674_523-673delinsTA