Canonical Allele Identifier: CA451020770

Gene: PHIP

Linked Data

• MyVariant Identifiers: chr6:g.79752626T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042909T>A , CM000668.2:g.79042909T>A	GRCh38
NC_000006.11:g.79752626T>A , CM000668.1:g.79752626T>A	GRCh37
NC_000006.10:g.79809345T>A	NCBI36
NG_051932.1:g.40390A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700012.1:c.552A>T	ENSP00000514753.1:p.Arg184=
ENST00000700013.1:c.552A>T	ENSP00000514754.1:p.Arg184=
ENST00000700114.1:c.474A>T	ENSP00000514808.1:p.Arg158=
ENST00000700115.1:c.534A>T	ENSP00000514809.1:p.Arg178=
ENST00000700118.1:c.534A>T	ENSP00000514810.1:p.Arg178=
ENST00000700119.1:c.*345A>T	ENSP00000514811.1:n.*345A>T
ENST00000700120.1:n.462A>T
ENST00000275034.5:c.534A>T MANE Select	ENSP00000275034.3:p.Arg178=
ENST00000275034.4:c.534A>T	ENSP00000275034.3:p.Arg178=
NM_017934.5:c.534A>T	NP_060404.3:p.Arg178=
XM_005248729.3:c.534A>T	XP_005248786.1:p.Arg178=
XM_011535917.1:c.534A>T	XP_011534219.1:p.Arg178=
XM_011535918.1:c.18A>T	XP_011534220.1:p.Arg6=
XM_011535919.1:c.534A>T	XP_011534221.1:p.Arg178=
XR_942499.1:n.760A>T
NM_017934.6:c.534A>T	NP_060404.4:p.Arg178=
XM_005248729.5:c.534A>T	XP_005248786.1:p.Arg178=
XM_011535918.3:c.18A>T	XP_011534220.1:p.Arg6=
XM_017010989.2:c.-1196A>T	XP_016866478.1:n.-1196A>T
XM_017010990.2:c.-1196A>T	XP_016866479.1:n.-1196A>T
NM_017934.7:c.534A>T MANE Select	NP_060404.4:p.Arg178=