Canonical Allele Identifier: CA364643421
Gene: PHIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79042992A>G , CM000668.2:g.79042992A>G GRCh38
NC_000006.11:g.79752709A>G , CM000668.1:g.79752709A>G GRCh37
NC_000006.10:g.79809428A>G NCBI36
NG_051932.1:g.40307T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700012.1:c.469T>C ENSP00000514753.1:p.Phe157Leu
ENST00000700013.1:c.469T>C ENSP00000514754.1:p.Phe157Leu
ENST00000700114.1:c.391T>C ENSP00000514808.1:p.Phe131Leu
ENST00000700115.1:c.451T>C ENSP00000514809.1:p.Phe151Leu
ENST00000700118.1:c.451T>C ENSP00000514810.1:p.Phe151Leu
ENST00000700119.1:c.*262T>C ENSP00000514811.1:n.*262T>C
ENST00000700120.1:n.379T>C
ENST00000275034.5:c.451T>C MANE Select ENSP00000275034.3:p.Phe151Leu
ENST00000275034.4:c.451T>C ENSP00000275034.3:p.Phe151Leu
NM_017934.5:c.451T>C NP_060404.3:p.Phe151Leu
XM_005248729.3:c.451T>C XP_005248786.1:p.Phe151Leu
XM_011535917.1:c.451T>C XP_011534219.1:p.Phe151Leu
XM_011535918.1:c.-66T>C XP_011534220.1:n.-66T>C
XM_011535919.1:c.451T>C XP_011534221.1:p.Phe151Leu
XR_942499.1:n.677T>C
NM_017934.6:c.451T>C NP_060404.4:p.Phe151Leu
XM_005248729.5:c.451T>C XP_005248786.1:p.Phe151Leu
XM_011535918.3:c.-66T>C XP_011534220.1:n.-66T>C
XM_017010989.2:c.-1279T>C XP_016866478.1:n.-1279T>C
XM_017010990.2:c.-1279T>C XP_016866479.1:n.-1279T>C
NM_017934.7:c.451T>C MANE Select NP_060404.4:p.Phe151Leu