Canonical Allele Identifier: CA2493890582

Gene: PLEKHH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43737868C= , CM000664.2:g.43737868C=	GRCh38
NC_000002.11:g.43965007C= , CM000664.1:g.43965007C=	GRCh37
NC_000002.10:g.43818511C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282406.9:c.2944-473C= MANE Select	ENSP00000282406.4:n.2944-473C=
ENST00000282406.8:c.2944-473C=	ENSP00000282406.4:n.2944-473C=
ENST00000405000.6:n.4870-473C=
ENST00000405223.6:n.3024-473C=
ENST00000480103.5:n.63-473C=
NM_172069.3:c.2944-473C=	NP_742066.2:n.2944-473C=
XM_011532539.1:c.1255-473C=	XP_011530841.1:n.1255-473C=
XR_244924.1:n.3027-473C=
XR_426981.1:n.3027-473C=
XR_939656.1:n.3027-473C=
XR_939657.1:n.3017-473C=
XM_017003351.2:c.2821-473C=	XP_016858840.1:n.2821-473C=
XM_017003353.1:c.1255-473C=	XP_016858842.1:n.1255-473C=
XM_024452695.1:c.2749-473C=	XP_024308463.1:n.2749-473C=
XR_001738620.1:n.3027-473C=
XR_001738621.1:n.3027-473C=
XR_001738622.1:n.3027-473C=
XR_426981.2:n.3027-473C=
XR_939657.2:n.3017-473C=
NM_172069.4:c.2944-473C= MANE Select	NP_742066.2:n.2944-473C=