Canonical Allele Identifier: CA1459162461

Gene: NMU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55601098_55601099delinsTC , CM000666.2:g.55601098_55601099delinsTC	GRCh38
NC_000004.11:g.56467265_56467266delinsTC , CM000666.1:g.56467265_56467266delinsTC	GRCh37
NC_000004.10:g.56162022_56162023delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264218.7:c.436-524_436-523delinsGA MANE Select	ENSP00000264218.3:n.436-524_436-523delins...
ENST00000505262.5:c.355-524_355-523delinsGA	ENSP00000424246.1:n.355-524_355-523delins...
ENST00000507338.1:c.361-524_361-523delinsGA	ENSP00000422870.1:n.361-524_361-523delins...
ENST00000509371.1:n.200-524_200-523delinsGA
ENST00000511469.5:c.388-524_388-523delinsGA	ENSP00000422399.1:n.388-524_388-523delins...
ENST00000515325.5:n.428-524_428-523delinsGA
NM_001292045.1:c.388-524_388-523delinsGA	NP_001278974.1:n.388-524_388-523delinsGA
NM_001292046.1:c.361-524_361-523delinsGA	NP_001278975.1:n.361-524_361-523delinsGA
NM_006681.3:c.436-524_436-523delinsGA	NP_006672.1:n.436-524_436-523delinsGA
NR_120489.1:n.428-524_428-523delinsGA
XM_011534367.1:c.385-524_385-523delinsGA	XP_011532669.1:n.385-524_385-523delinsGA
XM_011534368.1:c.334-524_334-523delinsGA	XP_011532670.1:n.334-524_334-523delinsGA
XM_011534367.2:c.385-524_385-523delinsGA	XP_011532669.1:n.385-524_385-523delinsGA
XM_011534368.3:c.334-524_334-523delinsGA	XP_011532670.1:n.334-524_334-523delinsGA
NM_006681.4:c.436-524_436-523delinsGA MANE Select	NP_006672.1:n.436-524_436-523delinsGA
NM_001292045.2:c.388-524_388-523delinsGA	NP_001278974.1:n.388-524_388-523delinsGA
NM_001292046.2:c.361-524_361-523delinsGA	NP_001278975.1:n.361-524_361-523delinsGA
NR_120489.2:n.523-524_523-523delinsGA