Canonical Allele Identifier: CA1640411179
Gene: PHIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79025584T= , CM000668.2:g.79025584T= GRCh38
NC_000006.11:g.79735301T= , CM000668.1:g.79735301T= GRCh37
NC_000006.10:g.79792020T= NCBI36
NG_051932.1:g.57715A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700012.1:c.876A= ENSP00000514753.1:p.Leu292=
ENST00000700013.1:c.876A= ENSP00000514754.1:p.Leu292=
ENST00000700114.1:c.798A= ENSP00000514808.1:p.Leu266=
ENST00000700115.1:c.858A= ENSP00000514809.1:p.Leu286=
ENST00000700118.1:c.858A= ENSP00000514810.1:p.Leu286=
ENST00000700119.1:c.*669A= ENSP00000514811.1:n.*669A=
ENST00000275034.5:c.858A= MANE Select ENSP00000275034.3:p.Leu286=
ENST00000275034.4:c.858A= ENSP00000275034.3:p.Leu286=
NM_017934.5:c.858A= NP_060404.3:p.Leu286=
XM_005248729.3:c.858A= XP_005248786.1:p.Leu286=
XM_011535917.1:c.858A= XP_011534219.1:p.Leu286=
XM_011535918.1:c.342A= XP_011534220.1:p.Leu114=
XM_011535919.1:c.858A= XP_011534221.1:p.Leu286=
XR_942499.1:n.1084A=
NM_017934.6:c.858A= NP_060404.4:p.Leu286=
XM_005248729.5:c.858A= XP_005248786.1:p.Leu286=
XM_011535918.3:c.342A= XP_011534220.1:p.Leu114=
XM_017010989.2:c.-872A= XP_016866478.1:n.-872A=
XM_017010990.2:c.-872A= XP_016866479.1:n.-872A=
NM_017934.7:c.858A= MANE Select NP_060404.4:p.Leu286=