Canonical Allele Identifier: CA364643200

Gene: PHIP

Linked Data

• gnomAD v4: 6-79042930-C-A
• MyVariant Identifiers: chr6:g.79752647C>A (hg19) ; chr6:g.79042930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042930C>A , CM000668.2:g.79042930C>A	GRCh38
NC_000006.11:g.79752647C>A , CM000668.1:g.79752647C>A	GRCh37
NC_000006.10:g.79809366C>A	NCBI36
NG_051932.1:g.40369G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.531G>T	ENSP00000514753.1:p.Gln177His
ENST00000700013.1:c.531G>T	ENSP00000514754.1:p.Gln177His
ENST00000700114.1:c.453G>T	ENSP00000514808.1:p.Gln151His
ENST00000700115.1:c.513G>T	ENSP00000514809.1:p.Gln171His
ENST00000700118.1:c.513G>T	ENSP00000514810.1:p.Gln171His
ENST00000700119.1:c.*324G>T	ENSP00000514811.1:n.*324G>T
ENST00000700120.1:n.441G>T
ENST00000275034.5:c.513G>T MANE Select	ENSP00000275034.3:p.Gln171His
ENST00000275034.4:c.513G>T	ENSP00000275034.3:p.Gln171His
NM_017934.5:c.513G>T	NP_060404.3:p.Gln171His
XM_005248729.3:c.513G>T	XP_005248786.1:p.Gln171His
XM_011535917.1:c.513G>T	XP_011534219.1:p.Gln171His
XM_011535918.1:c.-4G>T	XP_011534220.1:n.-4G>T
XM_011535919.1:c.513G>T	XP_011534221.1:p.Gln171His
XR_942499.1:n.739G>T
NM_017934.6:c.513G>T	NP_060404.4:p.Gln171His
XM_005248729.5:c.513G>T	XP_005248786.1:p.Gln171His
XM_011535918.3:c.-4G>T	XP_011534220.1:n.-4G>T
XM_017010989.2:c.-1217G>T	XP_016866478.1:n.-1217G>T
XM_017010990.2:c.-1217G>T	XP_016866479.1:n.-1217G>T
NM_017934.7:c.513G>T MANE Select	NP_060404.4:p.Gln171His