Canonical Allele Identifier: CA2679476921

Gene: PHIP

Linked Data

• gnomAD v4: 6-79025688-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79025688C>A , CM000668.2:g.79025688C>A	GRCh38
NC_000006.11:g.79735405C>A , CM000668.1:g.79735405C>A	GRCh37
NC_000006.10:g.79792124C>A	NCBI36
NG_051932.1:g.57611G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.841-69G>T	ENSP00000514753.1:n.841-69G>T
ENST00000700013.1:c.841-69G>T	ENSP00000514754.1:n.841-69G>T
ENST00000700114.1:c.763-69G>T	ENSP00000514808.1:n.763-69G>T
ENST00000700115.1:c.823-69G>T	ENSP00000514809.1:n.823-69G>T
ENST00000700118.1:c.823-69G>T	ENSP00000514810.1:n.823-69G>T
ENST00000700119.1:c.*634-69G>T	ENSP00000514811.1:n.*634-69G>T
ENST00000275034.5:c.823-69G>T MANE Select	ENSP00000275034.3:n.823-69G>T
ENST00000275034.4:c.823-69G>T	ENSP00000275034.3:n.823-69G>T
NM_017934.5:c.823-69G>T	NP_060404.3:n.823-69G>T
XM_005248729.3:c.823-69G>T	XP_005248786.1:n.823-69G>T
XM_011535917.1:c.823-69G>T	XP_011534219.1:n.823-69G>T
XM_011535918.1:c.307-69G>T	XP_011534220.1:n.307-69G>T
XM_011535919.1:c.823-69G>T	XP_011534221.1:n.823-69G>T
XR_942499.1:n.1049-69G>T
NM_017934.6:c.823-69G>T	NP_060404.4:n.823-69G>T
XM_005248729.5:c.823-69G>T	XP_005248786.1:n.823-69G>T
XM_011535918.3:c.307-69G>T	XP_011534220.1:n.307-69G>T
XM_017010989.2:c.-907-69G>T	XP_016866478.1:n.-907-69G>T
XM_017010990.2:c.-907-69G>T	XP_016866479.1:n.-907-69G>T
NM_017934.7:c.823-69G>T MANE Select	NP_060404.4:n.823-69G>T