Canonical Allele Identifier: CA781311009

Gene: PHLPP1

Linked Data

• dbSNP Id: rs1223246854
• MyVariant Identifiers: chr18:g.60440921A>G (hg19) ; chr18:g.62773688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773688A>G , CM000680.2:g.62773688A>G	GRCh38
NC_000018.9:g.60440921A>G , CM000680.1:g.60440921A>G	GRCh37
NC_000018.8:g.58591901A>G	NCBI36
NG_031923.1:g.63250A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262719.10:c.1577-56347A>G MANE Select	ENSP00000262719.4:n.1577-56347A>G
ENST00000262719.9:c.1577-56347A>G	ENSP00000262719.4:n.1577-56347A>G
NM_194449.3:c.1577-56347A>G	NP_919431.2:n.1577-56347A>G
XM_011525886.1:c.1577-56347A>G	XP_011524188.1:n.1577-56347A>G
XR_935564.1:n.212+128T>C
XR_935565.1:n.212+128T>C
XR_935566.1:n.212+128T>C
XR_935567.1:n.212+128T>C
XR_935568.1:n.212+128T>C
XR_935569.1:n.212+128T>C
XM_024451105.1:c.-48+32169A>G	XP_024306873.1:n.-48+32169A>G
XR_001753474.2:n.40+128T>C
NM_194449.4:c.1577-56347A>G MANE Select	NP_919431.2:n.1577-56347A>G