Canonical Allele Identifier: CA1090927308
Gene: PHIP HGNC NCBI

Linked Data

dbSNP Id: rs1771356261

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79025586_79025587del , CM000668.2:g.79025586_79025587del GRCh38
NC_000006.11:g.79735303_79735304del , CM000668.1:g.79735303_79735304del GRCh37
NC_000006.10:g.79792022_79792023del NCBI36
NG_051932.1:g.57713_57714del

Transcript Alleles

HGVS Amino-acid change
ENST00000700012.1:c.874_875del ENSP00000514753.1:p.Leu292IlefsTer20
ENST00000700013.1:c.874_875del ENSP00000514754.1:p.Leu292IlefsTer20
ENST00000700114.1:c.796_797del ENSP00000514808.1:p.Leu266IlefsTer20
ENST00000700115.1:c.856_857del ENSP00000514809.1:p.Leu286IlefsTer20
ENST00000700118.1:c.856_857del ENSP00000514810.1:p.Leu286IlefsTer20
ENST00000700119.1:c.*667_*668del ENSP00000514811.1:n.*667_*668del
ENST00000275034.5:c.856_857del MANE Select ENSP00000275034.3:p.Leu286IlefsTer20
ENST00000275034.4:c.856_857del ENSP00000275034.3:p.Leu286IlefsTer20
NM_017934.5:c.856_857del NP_060404.3:p.Leu286IlefsTer20
XM_005248729.3:c.856_857del XP_005248786.1:p.Leu286IlefsTer20
XM_011535917.1:c.856_857del XP_011534219.1:p.Leu286IlefsTer20
XM_011535918.1:c.340_341del XP_011534220.1:p.Leu114IlefsTer20
XM_011535919.1:c.856_857del XP_011534221.1:p.Leu286IlefsTer20
XR_942499.1:n.1082_1083del
NM_017934.6:c.856_857del NP_060404.4:p.Leu286IlefsTer20
XM_005248729.5:c.856_857del XP_005248786.1:p.Leu286IlefsTer20
XM_011535918.3:c.340_341del XP_011534220.1:p.Leu114IlefsTer20
XM_017010989.2:c.-874_-873del XP_016866478.1:n.-874_-873del
XM_017010990.2:c.-874_-873del XP_016866479.1:n.-874_-873del
NM_017934.7:c.856_857del MANE Select NP_060404.4:p.Leu286IlefsTer20