Canonical Allele Identifier: CA2308472268
Gene: PHLPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.62773631C= , CM000680.2:g.62773631C= GRCh38
NC_000018.9:g.60440864C= , CM000680.1:g.60440864C= GRCh37
NC_000018.8:g.58591844C= NCBI36
NG_031923.1:g.63193C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262719.10:c.1576+56372C= MANE Select ENSP00000262719.4:n.1576+56372C=
ENST00000262719.9:c.1576+56372C= ENSP00000262719.4:n.1576+56372C=
NM_194449.3:c.1576+56372C= NP_919431.2:n.1576+56372C=
XM_011525886.1:c.1576+56372C= XP_011524188.1:n.1576+56372C=
XR_935564.1:n.212+185G=
XR_935565.1:n.212+185G=
XR_935566.1:n.212+185G=
XR_935567.1:n.212+185G=
XR_935568.1:n.212+185G=
XR_935569.1:n.212+185G=
XM_024451105.1:c.-48+32112C= XP_024306873.1:n.-48+32112C=
XR_001753474.2:n.40+185G=
NM_194449.4:c.1576+56372C= MANE Select NP_919431.2:n.1576+56372C=