Canonical Allele Identifier: CA141874959

Gene: PHIP

Linked Data

• dbSNP Id: rs1010881164
• MyVariant Identifiers: chr6:g.79752939A>C (hg19) ; chr6:g.79043222A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79043222A>C , CM000668.2:g.79043222A>C	GRCh38
NC_000006.11:g.79752939A>C , CM000668.1:g.79752939A>C	GRCh37
NC_000006.10:g.79809658A>C	NCBI36
NG_051932.1:g.40077T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.458-219T>G	ENSP00000514753.1:n.458-219T>G
ENST00000700013.1:c.458-219T>G	ENSP00000514754.1:n.458-219T>G
ENST00000700114.1:c.380-219T>G	ENSP00000514808.1:n.380-219T>G
ENST00000700115.1:c.440-219T>G	ENSP00000514809.1:n.440-219T>G
ENST00000700118.1:c.440-219T>G	ENSP00000514810.1:n.440-219T>G
ENST00000700119.1:c.*251-219T>G	ENSP00000514811.1:n.*251-219T>G
ENST00000700120.1:n.368-219T>G
ENST00000275034.5:c.440-219T>G MANE Select	ENSP00000275034.3:n.440-219T>G
ENST00000275034.4:c.440-219T>G	ENSP00000275034.3:n.440-219T>G
NM_017934.5:c.440-219T>G	NP_060404.3:n.440-219T>G
XM_005248729.3:c.440-219T>G	XP_005248786.1:n.440-219T>G
XM_011535917.1:c.440-219T>G	XP_011534219.1:n.440-219T>G
XM_011535918.1:c.-77-219T>G	XP_011534220.1:n.-77-219T>G
XM_011535919.1:c.440-219T>G	XP_011534221.1:n.440-219T>G
XR_942499.1:n.666-219T>G
NM_017934.6:c.440-219T>G	NP_060404.4:n.440-219T>G
XM_005248729.5:c.440-219T>G	XP_005248786.1:n.440-219T>G
XM_011535918.3:c.-77-219T>G	XP_011534220.1:n.-77-219T>G
XM_017010989.2:c.-1290-219T>G	XP_016866478.1:n.-1290-219T>G
XM_017010990.2:c.-1290-219T>G	XP_016866479.1:n.-1290-219T>G
NM_017934.7:c.440-219T>G MANE Select	NP_060404.4:n.440-219T>G