Canonical Allele Identifier: CA1640411181
Gene: PHIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79025587A= , CM000668.2:g.79025587A= GRCh38
NC_000006.11:g.79735304A= , CM000668.1:g.79735304A= GRCh37
NC_000006.10:g.79792023A= NCBI36
NG_051932.1:g.57712T=

Transcript Alleles

HGVS Amino-acid change
ENST00000700012.1:c.873T= ENSP00000514753.1:p.Tyr291=
ENST00000700013.1:c.873T= ENSP00000514754.1:p.Tyr291=
ENST00000700114.1:c.795T= ENSP00000514808.1:p.Tyr265=
ENST00000700115.1:c.855T= ENSP00000514809.1:p.Tyr285=
ENST00000700118.1:c.855T= ENSP00000514810.1:p.Tyr285=
ENST00000700119.1:c.*666T= ENSP00000514811.1:n.*666T=
ENST00000275034.5:c.855T= MANE Select ENSP00000275034.3:p.Tyr285=
ENST00000275034.4:c.855T= ENSP00000275034.3:p.Tyr285=
NM_017934.5:c.855T= NP_060404.3:p.Tyr285=
XM_005248729.3:c.855T= XP_005248786.1:p.Tyr285=
XM_011535917.1:c.855T= XP_011534219.1:p.Tyr285=
XM_011535918.1:c.339T= XP_011534220.1:p.Tyr113=
XM_011535919.1:c.855T= XP_011534221.1:p.Tyr285=
XR_942499.1:n.1081T=
NM_017934.6:c.855T= NP_060404.4:p.Tyr285=
XM_005248729.5:c.855T= XP_005248786.1:p.Tyr285=
XM_011535918.3:c.339T= XP_011534220.1:p.Tyr113=
XM_017010989.2:c.-875T= XP_016866478.1:n.-875T=
XM_017010990.2:c.-875T= XP_016866479.1:n.-875T=
NM_017934.7:c.855T= MANE Select NP_060404.4:p.Tyr285=