Canonical Allele Identifier: CA301981973

Gene: PHLPP1

Linked Data

• dbSNP Id: rs560643217
• gnomAD v3: 18-62773622-G-A
• gnomAD v4: 18-62773622-G-A
• MyVariant Identifiers: chr18:g.60440855G>A (hg19) ; chr18:g.62773622G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773622G>A , CM000680.2:g.62773622G>A	GRCh38
NC_000018.9:g.60440855G>A , CM000680.1:g.60440855G>A	GRCh37
NC_000018.8:g.58591835G>A	NCBI36
NG_031923.1:g.63184G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262719.10:c.1576+56363G>A MANE Select	ENSP00000262719.4:n.1576+56363G>A
ENST00000262719.9:c.1576+56363G>A	ENSP00000262719.4:n.1576+56363G>A
NM_194449.3:c.1576+56363G>A	NP_919431.2:n.1576+56363G>A
XM_011525886.1:c.1576+56363G>A	XP_011524188.1:n.1576+56363G>A
XR_935564.1:n.212+194C>T
XR_935565.1:n.212+194C>T
XR_935566.1:n.212+194C>T
XR_935567.1:n.212+194C>T
XR_935568.1:n.212+194C>T
XR_935569.1:n.212+194C>T
XM_024451105.1:c.-48+32103G>A	XP_024306873.1:n.-48+32103G>A
XR_001753474.2:n.40+194C>T
NM_194449.4:c.1576+56363G>A MANE Select	NP_919431.2:n.1576+56363G>A