Canonical Allele Identifier: CA364638358

Gene: PHIP

Linked Data

• MyVariant Identifiers: chr6:g.79735307T>A (hg19) ; chr6:g.79025590T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79025590T>A , CM000668.2:g.79025590T>A	GRCh38
NC_000006.11:g.79735307T>A , CM000668.1:g.79735307T>A	GRCh37
NC_000006.10:g.79792026T>A	NCBI36
NG_051932.1:g.57709A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700012.1:c.870A>T	ENSP00000514753.1:p.Arg290Ser
ENST00000700013.1:c.870A>T	ENSP00000514754.1:p.Arg290Ser
ENST00000700114.1:c.792A>T	ENSP00000514808.1:p.Arg264Ser
ENST00000700115.1:c.852A>T	ENSP00000514809.1:p.Arg284Ser
ENST00000700118.1:c.852A>T	ENSP00000514810.1:p.Arg284Ser
ENST00000700119.1:c.*663A>T	ENSP00000514811.1:n.*663A>T
ENST00000275034.5:c.852A>T MANE Select	ENSP00000275034.3:p.Arg284Ser
ENST00000275034.4:c.852A>T	ENSP00000275034.3:p.Arg284Ser
NM_017934.5:c.852A>T	NP_060404.3:p.Arg284Ser
XM_005248729.3:c.852A>T	XP_005248786.1:p.Arg284Ser
XM_011535917.1:c.852A>T	XP_011534219.1:p.Arg284Ser
XM_011535918.1:c.336A>T	XP_011534220.1:p.Arg112Ser
XM_011535919.1:c.852A>T	XP_011534221.1:p.Arg284Ser
XR_942499.1:n.1078A>T
NM_017934.6:c.852A>T	NP_060404.4:p.Arg284Ser
XM_005248729.5:c.852A>T	XP_005248786.1:p.Arg284Ser
XM_011535918.3:c.336A>T	XP_011534220.1:p.Arg112Ser
XM_017010989.2:c.-878A>T	XP_016866478.1:n.-878A>T
XM_017010990.2:c.-878A>T	XP_016866479.1:n.-878A>T
NM_017934.7:c.852A>T MANE Select	NP_060404.4:p.Arg284Ser