Canonical Allele Identifier: CA364633759

Gene: PHIP IRAK1BP1

Linked Data

• MyVariant Identifiers: chr6:g.79650991C>G (hg19) ; chr6:g.78941274C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.78941274C>G , CM000668.2:g.78941274C>G	GRCh38
NC_000006.11:g.79650991C>G , CM000668.1:g.79650991C>G	GRCh37
NC_000006.10:g.79707710C>G	NCBI36
NG_051932.1:g.142025G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700013.1:c.4903G>C (PHIP)	ENSP00000514754.1:p.Gly1635Arg
ENST00000700114.1:c.4825G>C (PHIP)	ENSP00000514808.1:p.Gly1609Arg
ENST00000700115.1:c.4882G>C (PHIP)	ENSP00000514809.1:p.Gly1628Arg
ENST00000700116.1:n.3084G>C (PHIP)
ENST00000700118.1:c.4924G>C (PHIP)	ENSP00000514810.1:p.Gly1642Arg
ENST00000700170.1:n.1484G>C (PHIP)
ENST00000700171.1:c.907G>C (PHIP)
ENST00000275034.5:c.4885G>C (PHIP) MANE Select	ENSP00000275034.3:p.Gly1629Arg
ENST00000275034.4:c.4885G>C (PHIP)	ENSP00000275034.3:p.Gly1629Arg
ENST00000479165.1:n.4966G>C (PHIP)
ENST00000606868.5:c.602-4134C>G (IRAK1BP1)	ENSP00000475570.1:n.602-4134C>G
NM_017934.5:c.4885G>C (PHIP)	NP_060404.3:p.Gly1629Arg
XM_005248729.3:c.4882G>C (PHIP)	XP_005248786.1:p.Gly1628Arg
XM_011535917.1:c.4732G>C (PHIP)	XP_011534219.1:p.Gly1578Arg
XM_011535918.1:c.4369G>C (PHIP)	XP_011534220.1:p.Gly1457Arg
NM_017934.6:c.4885G>C (PHIP)	NP_060404.4:p.Gly1629Arg
XM_005248729.5:c.4882G>C (PHIP)	XP_005248786.1:p.Gly1628Arg
XM_011535918.3:c.4369G>C (PHIP)	XP_011534220.1:p.Gly1457Arg
XM_017010989.2:c.3220G>C (PHIP)	XP_016866478.1:p.Gly1074Arg
XM_017010990.2:c.3220G>C (PHIP)	XP_016866479.1:p.Gly1074Arg
XR_001743162.1:n.817+5705C>G (IRAK1BP1)
NM_017934.7:c.4885G>C (PHIP) MANE Select	NP_060404.4:p.Gly1629Arg