Canonical Allele Identifier: CA1640421575

Gene: PHIP

Linked Data

• dbSNP Id: rs1772307414

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79043148T>G , CM000668.2:g.79043148T>G	GRCh38
NC_000006.11:g.79752865T>G , CM000668.1:g.79752865T>G	GRCh37
NC_000006.10:g.79809584T>G	NCBI36
NG_051932.1:g.40151A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.458-145A>C	ENSP00000514753.1:n.458-145A>C
ENST00000700013.1:c.458-145A>C	ENSP00000514754.1:n.458-145A>C
ENST00000700114.1:c.380-145A>C	ENSP00000514808.1:n.380-145A>C
ENST00000700115.1:c.440-145A>C	ENSP00000514809.1:n.440-145A>C
ENST00000700118.1:c.440-145A>C	ENSP00000514810.1:n.440-145A>C
ENST00000700119.1:c.*251-145A>C	ENSP00000514811.1:n.*251-145A>C
ENST00000700120.1:n.368-145A>C
ENST00000275034.5:c.440-145A>C MANE Select	ENSP00000275034.3:n.440-145A>C
ENST00000275034.4:c.440-145A>C	ENSP00000275034.3:n.440-145A>C
NM_017934.5:c.440-145A>C	NP_060404.3:n.440-145A>C
XM_005248729.3:c.440-145A>C	XP_005248786.1:n.440-145A>C
XM_011535917.1:c.440-145A>C	XP_011534219.1:n.440-145A>C
XM_011535918.1:c.-77-145A>C	XP_011534220.1:n.-77-145A>C
XM_011535919.1:c.440-145A>C	XP_011534221.1:n.440-145A>C
XR_942499.1:n.666-145A>C
NM_017934.6:c.440-145A>C	NP_060404.4:n.440-145A>C
XM_005248729.5:c.440-145A>C	XP_005248786.1:n.440-145A>C
XM_011535918.3:c.-77-145A>C	XP_011534220.1:n.-77-145A>C
XM_017010989.2:c.-1290-145A>C	XP_016866478.1:n.-1290-145A>C
XM_017010990.2:c.-1290-145A>C	XP_016866479.1:n.-1290-145A>C
NM_017934.7:c.440-145A>C MANE Select	NP_060404.4:n.440-145A>C