Canonical Allele Identifier: CA1640411159

Gene: PHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79025510G= , CM000668.2:g.79025510G=	GRCh38
NC_000006.11:g.79735227G= , CM000668.1:g.79735227G=	GRCh37
NC_000006.10:g.79791946G=	NCBI36
NG_051932.1:g.57789C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700012.1:c.941+9C=	ENSP00000514753.1:n.941+9C=
ENST00000700013.1:c.941+9C=	ENSP00000514754.1:n.941+9C=
ENST00000700114.1:c.863+9C=	ENSP00000514808.1:n.863+9C=
ENST00000700115.1:c.923+9C=	ENSP00000514809.1:n.923+9C=
ENST00000700118.1:c.923+9C=	ENSP00000514810.1:n.923+9C=
ENST00000700119.1:c.*734+9C=	ENSP00000514811.1:n.*734+9C=
ENST00000275034.5:c.923+9C= MANE Select	ENSP00000275034.3:n.923+9C=
ENST00000275034.4:c.923+9C=	ENSP00000275034.3:n.923+9C=
NM_017934.5:c.923+9C=	NP_060404.3:n.923+9C=
XM_005248729.3:c.923+9C=	XP_005248786.1:n.923+9C=
XM_011535917.1:c.923+9C=	XP_011534219.1:n.923+9C=
XM_011535918.1:c.407+9C=	XP_011534220.1:n.407+9C=
XM_011535919.1:c.923+9C=	XP_011534221.1:n.923+9C=
XR_942499.1:n.1149+9C=
NM_017934.6:c.923+9C=	NP_060404.4:n.923+9C=
XM_005248729.5:c.923+9C=	XP_005248786.1:n.923+9C=
XM_011535918.3:c.407+9C=	XP_011534220.1:n.407+9C=
XM_017010989.2:c.-807+9C=	XP_016866478.1:n.-807+9C=
XM_017010990.2:c.-807+9C=	XP_016866479.1:n.-807+9C=
NM_017934.7:c.923+9C= MANE Select	NP_060404.4:n.923+9C=