Canonical Allele Identifier: CA3589131

Gene: NHP2 RMND5B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178149872del , CM000667.2:g.178149872del	GRCh38
NC_000005.9:g.177576873del , CM000667.1:g.177576873del	GRCh37
NC_000005.8:g.177509479del	NCBI36
NG_011765.1:g.9094del , LRG_346:g.9094del

Transcript Alleles

HGVS	Amino-acid Change
NM_017838.4:c.337-29del (NHP2) MANE Select	NP_060308.1:n.337-29del
NM_022762.5:c.*1840del (RMND5B) MANE Select	NP_073599.2:n.*1840del
ENST00000274606.8:c.337-29del (NHP2) MANE Select	ENSP00000274606.4:n.337-29del
ENST00000313386.9:c.*1840del (RMND5B) MANE Select	ENSP00000320623.4:n.*1840del
NM_001034833.1:c.231-29del (NHP2)	NP_001030005.1:n.231-29del
NM_001034833.2:c.231-29del (NHP2)	NP_001030005.1:n.231-29del
NM_001288794.2:c.*1840del (RMND5B)	NP_001275723.1:n.*1840del
NM_001288795.2:c.*1840del (RMND5B)	NP_001275724.1:n.*1840del
NM_001396110.1:c.465-29del (NHP2)	NP_001383039.1:n.465-29del
NM_017838.3:c.337-29del , LRG_346t1:c.337-29del (NHP2)	NP_060308.1:n.337-29del
ENST00000274606.7:c.337-29del (NHP2)	ENSP00000274606.3:n.337-29del
ENST00000314397.8:c.231-29del (NHP2)	ENSP00000366276.2:n.231-29del
ENST00000314397.9:c.231-29del (NHP2)	ENSP00000366276.2:n.231-29del
ENST00000513162.5:n.4131del (RMND5B)
ENST00000515098.5:c.*1840del (RMND5B)	ENSP00000420875.1:n.*1840del
ENST00000697323.1:n.238-29del (NHP2)