Canonical Allele Identifier: CA364643104

Gene: PHIP

Linked Data

• MyVariant Identifiers: chr6:g.79752624A>G (hg19) ; chr6:g.79042907A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042907A>G , CM000668.2:g.79042907A>G	GRCh38
NC_000006.11:g.79752624A>G , CM000668.1:g.79752624A>G	GRCh37
NC_000006.10:g.79809343A>G	NCBI36
NG_051932.1:g.40392T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000700012.1:c.554T>C	ENSP00000514753.1:p.Ile185Thr
ENST00000700013.1:c.554T>C	ENSP00000514754.1:p.Ile185Thr
ENST00000700114.1:c.476T>C	ENSP00000514808.1:p.Ile159Thr
ENST00000700115.1:c.536T>C	ENSP00000514809.1:p.Ile179Thr
ENST00000700118.1:c.536T>C	ENSP00000514810.1:p.Ile179Thr
ENST00000700119.1:c.*347T>C	ENSP00000514811.1:n.*347T>C
ENST00000700120.1:n.464T>C
ENST00000275034.5:c.536T>C MANE Select	ENSP00000275034.3:p.Ile179Thr
ENST00000275034.4:c.536T>C	ENSP00000275034.3:p.Ile179Thr
NM_017934.5:c.536T>C	NP_060404.3:p.Ile179Thr
XM_005248729.3:c.536T>C	XP_005248786.1:p.Ile179Thr
XM_011535917.1:c.536T>C	XP_011534219.1:p.Ile179Thr
XM_011535918.1:c.20T>C	XP_011534220.1:p.Ile7Thr
XM_011535919.1:c.536T>C	XP_011534221.1:p.Ile179Thr
XR_942499.1:n.762T>C
NM_017934.6:c.536T>C	NP_060404.4:p.Ile179Thr
XM_005248729.5:c.536T>C	XP_005248786.1:p.Ile179Thr
XM_011535918.3:c.20T>C	XP_011534220.1:p.Ile7Thr
XM_017010989.2:c.-1194T>C	XP_016866478.1:n.-1194T>C
XM_017010990.2:c.-1194T>C	XP_016866479.1:n.-1194T>C
NM_017934.7:c.536T>C MANE Select	NP_060404.4:p.Ile179Thr