Canonical Allele Identifier: CA451021132

Gene: PHIP

Linked Data

• MyVariant Identifiers: chr6:g.79752719C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79043002C>A , CM000668.2:g.79043002C>A	GRCh38
NC_000006.11:g.79752719C>A , CM000668.1:g.79752719C>A	GRCh37
NC_000006.10:g.79809438C>A	NCBI36
NG_051932.1:g.40297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.459G>T	ENSP00000514753.1:p.Ala153=
ENST00000700013.1:c.459G>T	ENSP00000514754.1:p.Ala153=
ENST00000700114.1:c.381G>T	ENSP00000514808.1:p.Ala127=
ENST00000700115.1:c.441G>T	ENSP00000514809.1:p.Ala147=
ENST00000700118.1:c.441G>T	ENSP00000514810.1:p.Ala147=
ENST00000700119.1:c.*252G>T	ENSP00000514811.1:n.*252G>T
ENST00000700120.1:n.369G>T
ENST00000275034.5:c.441G>T MANE Select	ENSP00000275034.3:p.Ala147=
ENST00000275034.4:c.441G>T	ENSP00000275034.3:p.Ala147=
NM_017934.5:c.441G>T	NP_060404.3:p.Ala147=
XM_005248729.3:c.441G>T	XP_005248786.1:p.Ala147=
XM_011535917.1:c.441G>T	XP_011534219.1:p.Ala147=
XM_011535918.1:c.-76G>T	XP_011534220.1:n.-76G>T
XM_011535919.1:c.441G>T	XP_011534221.1:p.Ala147=
XR_942499.1:n.667G>T
NM_017934.6:c.441G>T	NP_060404.4:p.Ala147=
XM_005248729.5:c.441G>T	XP_005248786.1:p.Ala147=
XM_011535918.3:c.-76G>T	XP_011534220.1:n.-76G>T
XM_017010989.2:c.-1289G>T	XP_016866478.1:n.-1289G>T
XM_017010990.2:c.-1289G>T	XP_016866479.1:n.-1289G>T
NM_017934.7:c.441G>T MANE Select	NP_060404.4:p.Ala147=