Canonical Allele Identifier: CA1640421582

Gene: PHIP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79043163A= , CM000668.2:g.79043163A=	GRCh38
NC_000006.11:g.79752880A= , CM000668.1:g.79752880A=	GRCh37
NC_000006.10:g.79809599A=	NCBI36
NG_051932.1:g.40136T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.458-160T=	ENSP00000514753.1:n.458-160T=
ENST00000700013.1:c.458-160T=	ENSP00000514754.1:n.458-160T=
ENST00000700114.1:c.380-160T=	ENSP00000514808.1:n.380-160T=
ENST00000700115.1:c.440-160T=	ENSP00000514809.1:n.440-160T=
ENST00000700118.1:c.440-160T=	ENSP00000514810.1:n.440-160T=
ENST00000700119.1:c.*251-160T=	ENSP00000514811.1:n.*251-160T=
ENST00000700120.1:n.368-160T=
ENST00000275034.5:c.440-160T= MANE Select	ENSP00000275034.3:n.440-160T=
ENST00000275034.4:c.440-160T=	ENSP00000275034.3:n.440-160T=
NM_017934.5:c.440-160T=	NP_060404.3:n.440-160T=
XM_005248729.3:c.440-160T=	XP_005248786.1:n.440-160T=
XM_011535917.1:c.440-160T=	XP_011534219.1:n.440-160T=
XM_011535918.1:c.-77-160T=	XP_011534220.1:n.-77-160T=
XM_011535919.1:c.440-160T=	XP_011534221.1:n.440-160T=
XR_942499.1:n.666-160T=
NM_017934.6:c.440-160T=	NP_060404.4:n.440-160T=
XM_005248729.5:c.440-160T=	XP_005248786.1:n.440-160T=
XM_011535918.3:c.-77-160T=	XP_011534220.1:n.-77-160T=
XM_017010989.2:c.-1290-160T=	XP_016866478.1:n.-1290-160T=
XM_017010990.2:c.-1290-160T=	XP_016866479.1:n.-1290-160T=
NM_017934.7:c.440-160T= MANE Select	NP_060404.4:n.440-160T=