Canonical Allele Identifier: CA849890840

Gene: PHYHIP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22230919A>T , CM000670.2:g.22230919A>T	GRCh38
NC_000008.10:g.22088432A>T , CM000670.1:g.22088432A>T	GRCh37
NC_000008.9:g.22144377A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454243.7:c.-30+877T>A MANE Select	ENSP00000415491.2:n.-30+877T>A
ENST00000321613.7:c.-152+877T>A	ENSP00000320017.3:n.-152+877T>A
ENST00000454243.6:c.-30+877T>A	ENSP00000415491.2:n.-30+877T>A
NM_001099335.1:c.-152+877T>A	NP_001092805.1:n.-152+877T>A
NM_014759.3:c.-30+877T>A	NP_055574.3:n.-30+877T>A
XM_006716416.1:c.-30+877T>A	XP_006716479.1:n.-30+877T>A
XR_247134.2:n.338+877T>A
NM_001363311.1:c.-152+877T>A	NP_001350240.1:n.-152+877T>A
NM_001363312.1:c.-30+877T>A	NP_001350241.1:n.-30+877T>A
NR_156475.1:n.557+877T>A
NM_014759.4:c.-30+877T>A	NP_055574.3:n.-30+877T>A
NM_014759.5:c.-30+877T>A MANE Select	NP_055574.3:n.-30+877T>A
NM_001099335.2:c.-152+877T>A	NP_001092805.1:n.-152+877T>A
NM_001363311.2:c.-152+877T>A	NP_001350240.1:n.-152+877T>A
NM_001363312.2:c.-30+877T>A	NP_001350241.1:n.-30+877T>A
NR_156475.2:n.304+877T>A