Canonical Allele Identifier: CA781310990

Gene: PHLPP1

Linked Data

• dbSNP Id: rs1405718556
• MyVariant Identifiers: chr18:g.60440845del (hg19) ; chr18:g.62773612del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773612del , CM000680.2:g.62773612del	GRCh38
NC_000018.9:g.60440845del , CM000680.1:g.60440845del	GRCh37
NC_000018.8:g.58591825del	NCBI36
NG_031923.1:g.63174del

Transcript Alleles

HGVS	Amino-acid change
ENST00000262719.10:c.1576+56353del MANE Select	ENSP00000262719.4:n.1576+56353del
ENST00000262719.9:c.1576+56353del	ENSP00000262719.4:n.1576+56353del
NM_194449.3:c.1576+56353del	NP_919431.2:n.1576+56353del
XM_011525886.1:c.1576+56353del	XP_011524188.1:n.1576+56353del
XR_935564.1:n.212+204del
XR_935565.1:n.212+204del
XR_935566.1:n.212+204del
XR_935567.1:n.212+204del
XR_935568.1:n.212+204del
XR_935569.1:n.212+204del
XM_024451105.1:c.-48+32093del	XP_024306873.1:n.-48+32093del
XR_001753474.2:n.40+204del
NM_194449.4:c.1576+56353del MANE Select	NP_919431.2:n.1576+56353del