Canonical Allele Identifier: CA2308472258

Gene: PHLPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773611_62773612delinsTC , CM000680.2:g.62773611_62773612delinsTC	GRCh38
NC_000018.9:g.60440844_60440845delinsTC , CM000680.1:g.60440844_60440845delinsTC	GRCh37
NC_000018.8:g.58591824_58591825delinsTC	NCBI36
NG_031923.1:g.63173_63174delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262719.10:c.1576+56352_1576+56353delinsTC MANE Select	ENSP00000262719.4:n.1576+56352_1576+56353delinsTC
ENST00000262719.9:c.1576+56352_1576+56353delinsTC	ENSP00000262719.4:n.1576+56352_1576+56353delinsTC
NM_194449.3:c.1576+56352_1576+56353delinsTC	NP_919431.2:n.1576+56352_1576+56353delinsTC
XM_011525886.1:c.1576+56352_1576+56353delinsTC	XP_011524188.1:n.1576+56352_1576+56353delinsTC
XR_935564.1:n.212+204_212+205delinsGA
XR_935565.1:n.212+204_212+205delinsGA
XR_935566.1:n.212+204_212+205delinsGA
XR_935567.1:n.212+204_212+205delinsGA
XR_935568.1:n.212+204_212+205delinsGA
XR_935569.1:n.212+204_212+205delinsGA
XM_024451105.1:c.-48+32092_-48+32093delinsTC	XP_024306873.1:n.-48+32092_-48+32093delinsTC
XR_001753474.2:n.40+204_40+205delinsGA
NM_194449.4:c.1576+56352_1576+56353delinsTC MANE Select	NP_919431.2:n.1576+56352_1576+56353delinsTC