Canonical Allele Identifier: CA364632825
Gene: PHIP HGNC NCBI
IRAK1BP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.78940893A>G , CM000668.2:g.78940893A>G GRCh38
NC_000006.11:g.79650610A>G , CM000668.1:g.79650610A>G GRCh37
NC_000006.10:g.79707329A>G NCBI36
NG_051932.1:g.142406T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700013.1:c.5284T>C (PHIP) ENSP00000514754.1:p.Phe1762Leu
ENST00000700114.1:c.5206T>C (PHIP) ENSP00000514808.1:p.Phe1736Leu
ENST00000700115.1:c.5263T>C (PHIP) ENSP00000514809.1:p.Phe1755Leu
ENST00000700116.1:n.3465T>C (PHIP)
ENST00000700118.1:c.5305T>C (PHIP) ENSP00000514810.1:p.Phe1769Leu
ENST00000700170.1:n.1865T>C (PHIP)
ENST00000700171.1:c.1288T>C (PHIP)
ENST00000275034.5:c.5266T>C (PHIP) MANE Select ENSP00000275034.3:p.Phe1756Leu
ENST00000275034.4:c.5266T>C (PHIP) ENSP00000275034.3:p.Phe1756Leu
ENST00000479165.1:n.5347T>C (PHIP)
ENST00000606868.5:c.602-4515A>G (IRAK1BP1) ENSP00000475570.1:n.602-4515A>G
NM_017934.5:c.5266T>C (PHIP) NP_060404.3:p.Phe1756Leu
XM_005248729.3:c.5263T>C (PHIP) XP_005248786.1:p.Phe1755Leu
XM_011535917.1:c.5113T>C (PHIP) XP_011534219.1:p.Phe1705Leu
XM_011535918.1:c.4750T>C (PHIP) XP_011534220.1:p.Phe1584Leu
NM_017934.6:c.5266T>C (PHIP) NP_060404.4:p.Phe1756Leu
XM_005248729.5:c.5263T>C (PHIP) XP_005248786.1:p.Phe1755Leu
XM_011535918.3:c.4750T>C (PHIP) XP_011534220.1:p.Phe1584Leu
XM_017010989.2:c.3601T>C (PHIP) XP_016866478.1:p.Phe1201Leu
XM_017010990.2:c.3601T>C (PHIP) XP_016866479.1:p.Phe1201Leu
XR_001743162.1:n.817+5324A>G (IRAK1BP1)
NM_017934.7:c.5266T>C (PHIP) MANE Select NP_060404.4:p.Phe1756Leu