Canonical Allele Identifier: CA781310984

Gene: PHLPP1

Linked Data

• dbSNP Id: rs1405043493
• gnomAD v3: 18-62773604-G-T
• gnomAD v4: 18-62773604-G-T
• MyVariant Identifiers: chr18:g.60440837G>T (hg19) ; chr18:g.62773604G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62773604G>T , CM000680.2:g.62773604G>T	GRCh38
NC_000018.9:g.60440837G>T , CM000680.1:g.60440837G>T	GRCh37
NC_000018.8:g.58591817G>T	NCBI36
NG_031923.1:g.63166G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262719.10:c.1576+56345G>T MANE Select	ENSP00000262719.4:n.1576+56345G>T
ENST00000262719.9:c.1576+56345G>T	ENSP00000262719.4:n.1576+56345G>T
NM_194449.3:c.1576+56345G>T	NP_919431.2:n.1576+56345G>T
XM_011525886.1:c.1576+56345G>T	XP_011524188.1:n.1576+56345G>T
XR_935564.1:n.212+212C>A
XR_935565.1:n.212+212C>A
XR_935566.1:n.212+212C>A
XR_935567.1:n.212+212C>A
XR_935568.1:n.212+212C>A
XR_935569.1:n.212+212C>A
XM_024451105.1:c.-48+32085G>T	XP_024306873.1:n.-48+32085G>T
XR_001753474.2:n.40+212C>A
NM_194449.4:c.1576+56345G>T MANE Select	NP_919431.2:n.1576+56345G>T