Canonical Allele Identifier: CA617288

Gene: PLEKHM2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15731961C>T , CM000663.2:g.15731961C>T	GRCh38
NC_000001.10:g.16058456C>T , CM000663.1:g.16058456C>T	GRCh37
NC_000001.9:g.15931043C>T	NCBI36
NG_053033.1:g.55456C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375799.8:c.2538C>T MANE Select	ENSP00000364956.3:p.Ser846=
ENST00000642363.1:c.2415C>T	ENSP00000494591.1:p.Ser805=
ENST00000375793.2:c.2478C>T	ENSP00000364950.2:p.Ser826=
ENST00000375799.7:c.2538C>T	ENSP00000364956.3:p.Ser846=
ENST00000477849.1:n.354C>T
NM_015164.2:c.2538C>T	NP_055979.2:p.Ser846=
XM_005245790.2:c.2478C>T	XP_005245847.1:p.Ser826=
XM_005245791.3:c.1929C>T	XP_005245848.1:p.Ser643=
XR_946590.1:n.2769C>T
NM_015164.3:c.2538C>T	NP_055979.2:p.Ser846=
XM_005245790.4:c.2478C>T	XP_005245847.1:p.Ser826=
XM_005245791.4:c.1929C>T	XP_005245848.1:p.Ser643=
XM_017000757.1:c.2577C>T	XP_016856246.1:p.Ser859=
XM_017000758.1:c.2517C>T	XP_016856247.1:p.Ser839=
NM_015164.4:c.2538C>T MANE Select	NP_055979.2:p.Ser846=