Canonical Allele Identifier: CA1640421489
Gene: PHIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79042911G= , CM000668.2:g.79042911G= GRCh38
NC_000006.11:g.79752628G= , CM000668.1:g.79752628G= GRCh37
NC_000006.10:g.79809347G= NCBI36
NG_051932.1:g.40388C=

Transcript Alleles

HGVS Amino-acid change
ENST00000700012.1:c.550C= ENSP00000514753.1:p.Arg184=
ENST00000700013.1:c.550C= ENSP00000514754.1:p.Arg184=
ENST00000700114.1:c.472C= ENSP00000514808.1:p.Arg158=
ENST00000700115.1:c.532C= ENSP00000514809.1:p.Arg178=
ENST00000700118.1:c.532C= ENSP00000514810.1:p.Arg178=
ENST00000700119.1:c.*343C= ENSP00000514811.1:n.*343C=
ENST00000700120.1:n.460C=
ENST00000275034.5:c.532C= MANE Select ENSP00000275034.3:p.Arg178=
ENST00000275034.4:c.532C= ENSP00000275034.3:p.Arg178=
NM_017934.5:c.532C= NP_060404.3:p.Arg178=
XM_005248729.3:c.532C= XP_005248786.1:p.Arg178=
XM_011535917.1:c.532C= XP_011534219.1:p.Arg178=
XM_011535918.1:c.16C= XP_011534220.1:p.Arg6=
XM_011535919.1:c.532C= XP_011534221.1:p.Arg178=
XR_942499.1:n.758C=
NM_017934.6:c.532C= NP_060404.4:p.Arg178=
XM_005248729.5:c.532C= XP_005248786.1:p.Arg178=
XM_011535918.3:c.16C= XP_011534220.1:p.Arg6=
XM_017010989.2:c.-1198C= XP_016866478.1:n.-1198C=
XM_017010990.2:c.-1198C= XP_016866479.1:n.-1198C=
NM_017934.7:c.532C= MANE Select NP_060404.4:p.Arg178=