Canonical Allele Identifier: CA2562546760

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55601071_55601072insCTGTAGAAAT , CM000666.2:g.55601071_55601072insCTGTAGAAAT	GRCh38
NC_000004.11:g.56467238_56467239insCTGTAGAAAT , CM000666.1:g.56467238_56467239insCTGTAGAAAT	GRCh37
NC_000004.10:g.56161995_56161996insCTGTAGAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.436-496_436-495insTTTCTACAGA MANE Select	ENSP00000264218.3:n.436-496_436-495insTTTCTACAGA
ENST00000505262.5:c.355-496_355-495insTTTCTACAGA	ENSP00000424246.1:n.355-496_355-495insTTTCTACAGA
ENST00000507338.1:c.361-496_361-495insTTTCTACAGA	ENSP00000422870.1:n.361-496_361-495insTTTCTACAGA
ENST00000509371.1:n.200-496_200-495insTTTCTACAGA
ENST00000511469.5:c.388-496_388-495insTTTCTACAGA	ENSP00000422399.1:n.388-496_388-495insTTTCTACAGA
ENST00000515325.5:n.428-496_428-495insTTTCTACAGA
NM_001292045.1:c.388-496_388-495insTTTCTACAGA	NP_001278974.1:n.388-496_388-495insTTTCTACAGA
NM_001292046.1:c.361-496_361-495insTTTCTACAGA	NP_001278975.1:n.361-496_361-495insTTTCTACAGA
NM_006681.3:c.436-496_436-495insTTTCTACAGA	NP_006672.1:n.436-496_436-495insTTTCTACAGA
NR_120489.1:n.428-496_428-495insTTTCTACAGA
XM_011534367.1:c.385-496_385-495insTTTCTACAGA	XP_011532669.1:n.385-496_385-495insTTTCTACAGA
XM_011534368.1:c.334-496_334-495insTTTCTACAGA	XP_011532670.1:n.334-496_334-495insTTTCTACAGA
XM_011534367.2:c.385-496_385-495insTTTCTACAGA	XP_011532669.1:n.385-496_385-495insTTTCTACAGA
XM_011534368.3:c.334-496_334-495insTTTCTACAGA	XP_011532670.1:n.334-496_334-495insTTTCTACAGA
NM_006681.4:c.436-496_436-495insTTTCTACAGA MANE Select	NP_006672.1:n.436-496_436-495insTTTCTACAGA
NM_001292045.2:c.388-496_388-495insTTTCTACAGA	NP_001278974.1:n.388-496_388-495insTTTCTACAGA
NM_001292046.2:c.361-496_361-495insTTTCTACAGA	NP_001278975.1:n.361-496_361-495insTTTCTACAGA
NR_120489.2:n.523-496_523-495insTTTCTACAGA