Canonical Allele Identifier: CA2261852806

Gene: PLEKHM1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45436075C= , CM000679.2:g.45436075C=	GRCh38
NC_000017.10:g.43513441C= , CM000679.1:g.43513441C=	GRCh37
NC_000017.9:g.40869224C=	NCBI36
NG_012932.1:g.59706G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014798.3:c.*1783G= MANE Select	NP_055613.1:n.*1783G=
ENST00000430334.8:c.*1783G= MANE Select	ENSP00000389913.3:n.*1783G=
NM_014798.2:c.*1783G=	NP_055613.1:n.*1783G=
NR_027774.1:n.4876G=
NR_027774.2:n.4817G=
NR_027782.1:n.4739G=
NR_027782.2:n.4680G=
ENST00000430334.7:c.*1783G=	ENSP00000389913.3:n.*1783G=
ENST00000579197.5:c.*4514G=	ENSP00000462282.1:n.*4514G=
ENST00000580404.5:n.2456G=
XM_006722201.2:c.*1783G=	XP_006722264.1:n.*1783G=
XM_006722201.4:c.*1783G=	XP_006722264.1:n.*1783G=
XM_006722202.2:c.*1783G=	XP_006722265.1:n.*1783G=
XM_011525523.1:c.*35-1725G=	XP_011523825.1:n.*35-1725G=
XM_011525523.2:c.*35-1725G=	XP_011523825.1:n.*35-1725G=
XM_011525524.1:c.*1783G=	XP_011523826.1:n.*1783G=
XM_011525525.1:c.*1783G=	XP_011523827.1:n.*1783G=
XM_011525526.1:c.*1783G=	XP_011523828.1:n.*1783G=
XM_011525527.1:c.*1783G=	XP_011523829.1:n.*1783G=
XM_011525528.1:c.*1783G=	XP_011523830.1:n.*1783G=
XM_011525528.2:c.*1783G=	XP_011523830.1:n.*1783G=
XM_017025451.1:c.*1783G=	XP_016880940.1:n.*1783G=
XM_017025452.1:c.*1783G=	XP_016880941.1:n.*1783G=
XM_017025453.1:c.*1783G=	XP_016880942.1:n.*1783G=
XM_017025454.2:c.*1783G=	XP_016880943.1:n.*1783G=
XR_934624.1:n.5163G=
XR_934625.1:n.4926G=