Canonical Allele Identifier: CA2308472257

Gene: PHLPP1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773610_62773612delinsTTC , CM000680.2:g.62773610_62773612delinsTTC	GRCh38
NC_000018.9:g.60440843_60440845delinsTTC , CM000680.1:g.60440843_60440845delinsTTC	GRCh37
NC_000018.8:g.58591823_58591825delinsTTC	NCBI36
NG_031923.1:g.63172_63174delinsTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000262719.10:c.1576+56351_1576+56353delinsTTC MANE Select	ENSP00000262719.4:n.1576+56351_1576+56353delinsTTC
ENST00000262719.9:c.1576+56351_1576+56353delinsTTC	ENSP00000262719.4:n.1576+56351_1576+56353delinsTTC
NM_194449.3:c.1576+56351_1576+56353delinsTTC	NP_919431.2:n.1576+56351_1576+56353delinsTTC
XM_011525886.1:c.1576+56351_1576+56353delinsTTC	XP_011524188.1:n.1576+56351_1576+56353delinsTTC
XR_935564.1:n.212+204_212+206delinsGAA
XR_935565.1:n.212+204_212+206delinsGAA
XR_935566.1:n.212+204_212+206delinsGAA
XR_935567.1:n.212+204_212+206delinsGAA
XR_935568.1:n.212+204_212+206delinsGAA
XR_935569.1:n.212+204_212+206delinsGAA
XM_024451105.1:c.-48+32091_-48+32093delinsTTC	XP_024306873.1:n.-48+32091_-48+32093delinsTTC
XR_001753474.2:n.40+204_40+206delinsGAA
NM_194449.4:c.1576+56351_1576+56353delinsTTC MANE Select	NP_919431.2:n.1576+56351_1576+56353delinsTTC