Canonical Allele Identifier: CA364643439

Gene: PHIP

Linked Data

• gnomAD v4: 6-79042998-T-C
• MyVariant Identifiers: chr6:g.79752715T>C (hg19) ; chr6:g.79042998T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042998T>C , CM000668.2:g.79042998T>C	GRCh38
NC_000006.11:g.79752715T>C , CM000668.1:g.79752715T>C	GRCh37
NC_000006.10:g.79809434T>C	NCBI36
NG_051932.1:g.40301A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700012.1:c.463A>G	ENSP00000514753.1:p.Thr155Ala
ENST00000700013.1:c.463A>G	ENSP00000514754.1:p.Thr155Ala
ENST00000700114.1:c.385A>G	ENSP00000514808.1:p.Thr129Ala
ENST00000700115.1:c.445A>G	ENSP00000514809.1:p.Thr149Ala
ENST00000700118.1:c.445A>G	ENSP00000514810.1:p.Thr149Ala
ENST00000700119.1:c.*256A>G	ENSP00000514811.1:n.*256A>G
ENST00000700120.1:n.373A>G
ENST00000275034.5:c.445A>G MANE Select	ENSP00000275034.3:p.Thr149Ala
ENST00000275034.4:c.445A>G	ENSP00000275034.3:p.Thr149Ala
NM_017934.5:c.445A>G	NP_060404.3:p.Thr149Ala
XM_005248729.3:c.445A>G	XP_005248786.1:p.Thr149Ala
XM_011535917.1:c.445A>G	XP_011534219.1:p.Thr149Ala
XM_011535918.1:c.-72A>G	XP_011534220.1:n.-72A>G
XM_011535919.1:c.445A>G	XP_011534221.1:p.Thr149Ala
XR_942499.1:n.671A>G
NM_017934.6:c.445A>G	NP_060404.4:p.Thr149Ala
XM_005248729.5:c.445A>G	XP_005248786.1:p.Thr149Ala
XM_011535918.3:c.-72A>G	XP_011534220.1:n.-72A>G
XM_017010989.2:c.-1285A>G	XP_016866478.1:n.-1285A>G
XM_017010990.2:c.-1285A>G	XP_016866479.1:n.-1285A>G
NM_017934.7:c.445A>G MANE Select	NP_060404.4:p.Thr149Ala