Canonical Allele Identifier: CA2308472239

Gene: PHLPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773575C= , CM000680.2:g.62773575C=	GRCh38
NC_000018.9:g.60440808C= , CM000680.1:g.60440808C=	GRCh37
NC_000018.8:g.58591788C=	NCBI36
NG_031923.1:g.63137C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262719.10:c.1576+56316C= MANE Select	ENSP00000262719.4:n.1576+56316C=
ENST00000262719.9:c.1576+56316C=	ENSP00000262719.4:n.1576+56316C=
NM_194449.3:c.1576+56316C=	NP_919431.2:n.1576+56316C=
XM_011525886.1:c.1576+56316C=	XP_011524188.1:n.1576+56316C=
XR_935564.1:n.212+241G=
XR_935565.1:n.212+241G=
XR_935566.1:n.212+241G=
XR_935567.1:n.212+241G=
XR_935568.1:n.212+241G=
XR_935569.1:n.212+241G=
XM_024451105.1:c.-48+32056C=	XP_024306873.1:n.-48+32056C=
XR_001753474.2:n.40+241G=
NM_194449.4:c.1576+56316C= MANE Select	NP_919431.2:n.1576+56316C=