Canonical Allele Identifier: CA2308472260

Gene: PHLPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773622G= , CM000680.2:g.62773622G=	GRCh38
NC_000018.9:g.60440855G= , CM000680.1:g.60440855G=	GRCh37
NC_000018.8:g.58591835G=	NCBI36
NG_031923.1:g.63184G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262719.10:c.1576+56363G= MANE Select	ENSP00000262719.4:n.1576+56363G=
ENST00000262719.9:c.1576+56363G=	ENSP00000262719.4:n.1576+56363G=
NM_194449.3:c.1576+56363G=	NP_919431.2:n.1576+56363G=
XM_011525886.1:c.1576+56363G=	XP_011524188.1:n.1576+56363G=
XR_935564.1:n.212+194C=
XR_935565.1:n.212+194C=
XR_935566.1:n.212+194C=
XR_935567.1:n.212+194C=
XR_935568.1:n.212+194C=
XR_935569.1:n.212+194C=
XM_024451105.1:c.-48+32103G=	XP_024306873.1:n.-48+32103G=
XR_001753474.2:n.40+194C=
NM_194449.4:c.1576+56363G= MANE Select	NP_919431.2:n.1576+56363G=