Canonical Allele Identifier: CA362390898

Gene: NHP2 RMND5B

Linked Data

• ClinVar Variation Id: 1432972
• ClinVar RCV Id: RCV001944188
• dbSNP Id: rs121908091
• MyVariant Identifiers: chr5:g.177576716A>C (hg19) ; chr5:g.178149715A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178149715A>C , CM000667.2:g.178149715A>C	GRCh38
NC_000005.9:g.177576716A>C , CM000667.1:g.177576716A>C	GRCh37
NC_000005.8:g.177509322A>C	NCBI36
NG_011765.1:g.9246T>G , LRG_346:g.9246T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314397.9:c.*81T>G (NHP2)	ENSP00000366276.2:n.*81T>G
ENST00000697323.1:n.361T>G (NHP2)
ENST00000274606.8:c.460T>G (NHP2) MANE Select	ENSP00000274606.4:p.Ter154Gly
ENST00000313386.9:c.*1683A>C (RMND5B) MANE Select	ENSP00000320623.4:n.*1683A>C
ENST00000274606.7:c.460T>G (NHP2)	ENSP00000274606.3:p.Ter154Gly
ENST00000314397.8:c.*81T>G (NHP2)	ENSP00000366276.2:n.*81T>G
ENST00000513162.5:n.3974A>C (RMND5B)
ENST00000515098.5:c.*1683A>C (RMND5B)	ENSP00000420875.1:n.*1683A>C
NM_001034833.1:c.*81T>G (NHP2)	NP_001030005.1:n.*81T>G
NM_017838.3:c.460T>G , LRG_346t1:c.460T>G (NHP2)	NP_060308.1:p.Ter154Gly
NM_022762.5:c.*1683A>C (RMND5B) MANE Select	NP_073599.2:n.*1683A>C
NM_017838.4:c.460T>G (NHP2) MANE Select	NP_060308.1:p.Ter154Gly
NM_001034833.2:c.*81T>G (NHP2)	NP_001030005.1:n.*81T>G
NM_001288794.2:c.*1683A>C (RMND5B)	NP_001275723.1:n.*1683A>C
NM_001288795.2:c.*1683A>C (RMND5B)	NP_001275724.1:n.*1683A>C
NM_001396110.1:c.*81T>G (NHP2)	NP_001383039.1:n.*81T>G