Canonical Allele Identifier: CA3589186

Gene: NHP2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178150922C>T , CM000667.2:g.178150922C>T	GRCh38
NC_000005.9:g.177577923C>T , CM000667.1:g.177577923C>T	GRCh37
NC_000005.8:g.177510529C>T	NCBI36
NG_011765.1:g.8039G>A , LRG_346:g.8039G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314397.9:c.231-1084G>A	ENSP00000366276.2:n.231-1084G>A
ENST00000697323.1:n.203G>A
ENST00000274606.8:c.302G>A MANE Select	ENSP00000274606.4:p.Arg101Gln
ENST00000274606.7:c.302G>A	ENSP00000274606.3:p.Arg101Gln
ENST00000314397.8:c.231-1084G>A	ENSP00000366276.2:n.231-1084G>A
ENST00000502263.1:c.161G>A	ENSP00000431126.1:p.Arg54Gln
ENST00000511078.1:c.302G>A	ENSP00000423849.1:p.Arg101Gln
ENST00000514354.5:c.302G>A	ENSP00000423803.1:p.Arg101Gln
NM_001034833.1:c.231-1084G>A	NP_001030005.1:n.231-1084G>A
NM_017838.3:c.302G>A , LRG_346t1:c.302G>A	NP_060308.1:p.Arg101Gln
NM_017838.4:c.302G>A MANE Select	NP_060308.1:p.Arg101Gln
NM_001034833.2:c.231-1084G>A	NP_001030005.1:n.231-1084G>A
NM_001396110.1:c.302G>A	NP_001383039.1:p.Arg101Gln