Canonical Allele Identifier: CA2308472238
Gene: PHLPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1912860778
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.62773569A>T , CM000680.2:g.62773569A>T GRCh38
NC_000018.9:g.60440802A>T , CM000680.1:g.60440802A>T GRCh37
NC_000018.8:g.58591782A>T NCBI36
NG_031923.1:g.63131A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262719.10:c.1576+56310A>T MANE Select ENSP00000262719.4:n.1576+56310A>T
ENST00000262719.9:c.1576+56310A>T ENSP00000262719.4:n.1576+56310A>T
NM_194449.3:c.1576+56310A>T NP_919431.2:n.1576+56310A>T
XM_011525886.1:c.1576+56310A>T XP_011524188.1:n.1576+56310A>T
XR_935564.1:n.212+247T>A
XR_935565.1:n.212+247T>A
XR_935566.1:n.212+247T>A
XR_935567.1:n.212+247T>A
XR_935568.1:n.212+247T>A
XR_935569.1:n.212+247T>A
XM_024451105.1:c.-48+32050A>T XP_024306873.1:n.-48+32050A>T
XR_001753474.2:n.40+247T>A
NM_194449.4:c.1576+56310A>T MANE Select NP_919431.2:n.1576+56310A>T
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