Canonical Allele Identifier: CA451021044

Gene: PHIP

Linked Data

• MyVariant Identifiers: chr6:g.79752695C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042978C>A , CM000668.2:g.79042978C>A	GRCh38
NC_000006.11:g.79752695C>A , CM000668.1:g.79752695C>A	GRCh37
NC_000006.10:g.79809414C>A	NCBI36
NG_051932.1:g.40321G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.483G>T	ENSP00000514753.1:p.Leu161=
ENST00000700013.1:c.483G>T	ENSP00000514754.1:p.Leu161=
ENST00000700114.1:c.405G>T	ENSP00000514808.1:p.Leu135=
ENST00000700115.1:c.465G>T	ENSP00000514809.1:p.Leu155=
ENST00000700118.1:c.465G>T	ENSP00000514810.1:p.Leu155=
ENST00000700119.1:c.*276G>T	ENSP00000514811.1:n.*276G>T
ENST00000700120.1:n.393G>T
ENST00000275034.5:c.465G>T MANE Select	ENSP00000275034.3:p.Leu155=
ENST00000275034.4:c.465G>T	ENSP00000275034.3:p.Leu155=
NM_017934.5:c.465G>T	NP_060404.3:p.Leu155=
XM_005248729.3:c.465G>T	XP_005248786.1:p.Leu155=
XM_011535917.1:c.465G>T	XP_011534219.1:p.Leu155=
XM_011535918.1:c.-52G>T	XP_011534220.1:n.-52G>T
XM_011535919.1:c.465G>T	XP_011534221.1:p.Leu155=
XR_942499.1:n.691G>T
NM_017934.6:c.465G>T	NP_060404.4:p.Leu155=
XM_005248729.5:c.465G>T	XP_005248786.1:p.Leu155=
XM_011535918.3:c.-52G>T	XP_011534220.1:n.-52G>T
XM_017010989.2:c.-1265G>T	XP_016866478.1:n.-1265G>T
XM_017010990.2:c.-1265G>T	XP_016866479.1:n.-1265G>T
NM_017934.7:c.465G>T MANE Select	NP_060404.4:p.Leu155=