Canonical Allele Identifier: CA364643432

Gene: PHIP

Linked Data

• MyVariant Identifiers: chr6:g.79752712G>T (hg19) ; chr6:g.79042995G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042995G>T , CM000668.2:g.79042995G>T	GRCh38
NC_000006.11:g.79752712G>T , CM000668.1:g.79752712G>T	GRCh37
NC_000006.10:g.79809431G>T	NCBI36
NG_051932.1:g.40304C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.466C>A	ENSP00000514753.1:p.Leu156Met
ENST00000700013.1:c.466C>A	ENSP00000514754.1:p.Leu156Met
ENST00000700114.1:c.388C>A	ENSP00000514808.1:p.Leu130Met
ENST00000700115.1:c.448C>A	ENSP00000514809.1:p.Leu150Met
ENST00000700118.1:c.448C>A	ENSP00000514810.1:p.Leu150Met
ENST00000700119.1:c.*259C>A	ENSP00000514811.1:n.*259C>A
ENST00000700120.1:n.376C>A
ENST00000275034.5:c.448C>A MANE Select	ENSP00000275034.3:p.Leu150Met
ENST00000275034.4:c.448C>A	ENSP00000275034.3:p.Leu150Met
NM_017934.5:c.448C>A	NP_060404.3:p.Leu150Met
XM_005248729.3:c.448C>A	XP_005248786.1:p.Leu150Met
XM_011535917.1:c.448C>A	XP_011534219.1:p.Leu150Met
XM_011535918.1:c.-69C>A	XP_011534220.1:n.-69C>A
XM_011535919.1:c.448C>A	XP_011534221.1:p.Leu150Met
XR_942499.1:n.674C>A
NM_017934.6:c.448C>A	NP_060404.4:p.Leu150Met
XM_005248729.5:c.448C>A	XP_005248786.1:p.Leu150Met
XM_011535918.3:c.-69C>A	XP_011534220.1:n.-69C>A
XM_017010989.2:c.-1282C>A	XP_016866478.1:n.-1282C>A
XM_017010990.2:c.-1282C>A	XP_016866479.1:n.-1282C>A
NM_017934.7:c.448C>A MANE Select	NP_060404.4:p.Leu150Met