Canonical Allele Identifier: CA301981974
Gene: PHLPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1039804515

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.62773628A>C , CM000680.2:g.62773628A>C GRCh38
NC_000018.9:g.60440861A>C , CM000680.1:g.60440861A>C GRCh37
NC_000018.8:g.58591841A>C NCBI36
NG_031923.1:g.63190A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262719.10:c.1576+56369A>C MANE Select ENSP00000262719.4:n.1576+56369A>C
ENST00000262719.9:c.1576+56369A>C ENSP00000262719.4:n.1576+56369A>C
NM_194449.3:c.1576+56369A>C NP_919431.2:n.1576+56369A>C
XM_011525886.1:c.1576+56369A>C XP_011524188.1:n.1576+56369A>C
XR_935564.1:n.212+188T>G
XR_935565.1:n.212+188T>G
XR_935566.1:n.212+188T>G
XR_935567.1:n.212+188T>G
XR_935568.1:n.212+188T>G
XR_935569.1:n.212+188T>G
XM_024451105.1:c.-48+32109A>C XP_024306873.1:n.-48+32109A>C
XR_001753474.2:n.40+188T>G
NM_194449.4:c.1576+56369A>C MANE Select NP_919431.2:n.1576+56369A>C