Canonical Allele Identifier: CA2308472246
Gene: PHLPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1912861189

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.62773588T>A , CM000680.2:g.62773588T>A GRCh38
NC_000018.9:g.60440821T>A , CM000680.1:g.60440821T>A GRCh37
NC_000018.8:g.58591801T>A NCBI36
NG_031923.1:g.63150T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262719.10:c.1576+56329T>A MANE Select ENSP00000262719.4:n.1576+56329T>A
ENST00000262719.9:c.1576+56329T>A ENSP00000262719.4:n.1576+56329T>A
NM_194449.3:c.1576+56329T>A NP_919431.2:n.1576+56329T>A
XM_011525886.1:c.1576+56329T>A XP_011524188.1:n.1576+56329T>A
XR_935564.1:n.212+228A>T
XR_935565.1:n.212+228A>T
XR_935566.1:n.212+228A>T
XR_935567.1:n.212+228A>T
XR_935568.1:n.212+228A>T
XR_935569.1:n.212+228A>T
XM_024451105.1:c.-48+32069T>A XP_024306873.1:n.-48+32069T>A
XR_001753474.2:n.40+228A>T
NM_194449.4:c.1576+56329T>A MANE Select NP_919431.2:n.1576+56329T>A