Canonical Allele Identifier: CA364643116

Gene: PHIP

Linked Data

• ClinVar Variation Id: 489096
• ClinVar RCV Id: RCV000579147
• dbSNP Id: rs1554210094
• MyVariant Identifiers: chr6:g.79752628G>A (hg19) ; chr6:g.79042911G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79042911G>A , CM000668.2:g.79042911G>A	GRCh38
NC_000006.11:g.79752628G>A , CM000668.1:g.79752628G>A	GRCh37
NC_000006.10:g.79809347G>A	NCBI36
NG_051932.1:g.40388C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700012.1:c.550C>T	ENSP00000514753.1:p.Arg184Ter
ENST00000700013.1:c.550C>T	ENSP00000514754.1:p.Arg184Ter
ENST00000700114.1:c.472C>T	ENSP00000514808.1:p.Arg158Ter
ENST00000700115.1:c.532C>T	ENSP00000514809.1:p.Arg178Ter
ENST00000700118.1:c.532C>T	ENSP00000514810.1:p.Arg178Ter
ENST00000700119.1:c.*343C>T	ENSP00000514811.1:n.*343C>T
ENST00000700120.1:n.460C>T
ENST00000275034.5:c.532C>T MANE Select	ENSP00000275034.3:p.Arg178Ter
ENST00000275034.4:c.532C>T	ENSP00000275034.3:p.Arg178Ter
NM_017934.5:c.532C>T	NP_060404.3:p.Arg178Ter
XM_005248729.3:c.532C>T	XP_005248786.1:p.Arg178Ter
XM_011535917.1:c.532C>T	XP_011534219.1:p.Arg178Ter
XM_011535918.1:c.16C>T	XP_011534220.1:p.Arg6Ter
XM_011535919.1:c.532C>T	XP_011534221.1:p.Arg178Ter
XR_942499.1:n.758C>T
NM_017934.6:c.532C>T	NP_060404.4:p.Arg178Ter
XM_005248729.5:c.532C>T	XP_005248786.1:p.Arg178Ter
XM_011535918.3:c.16C>T	XP_011534220.1:p.Arg6Ter
XM_017010989.2:c.-1198C>T	XP_016866478.1:n.-1198C>T
XM_017010990.2:c.-1198C>T	XP_016866479.1:n.-1198C>T
NM_017934.7:c.532C>T MANE Select	NP_060404.4:p.Arg178Ter