Canonical Allele Identifier: CA1888247341

Gene: PRKCQ

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6508594T= , CM000672.2:g.6508594T=	GRCh38
NC_000010.10:g.6550556T= , CM000672.1:g.6550556T=	GRCh37
NC_000010.9:g.6590562T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000263125.10:c.319-1098A= MANE Select	ENSP00000263125.5:n.319-1098A=
ENST00000263125.9:c.319-1098A=	ENSP00000263125.5:n.319-1098A=
ENST00000397176.6:c.319-1098A=	ENSP00000380361.2:n.319-1098A=
ENST00000539722.5:c.4+2401A=	ENSP00000441752.1:n.4+2401A=
ENST00000610727.1:c.211-1098A=	ENSP00000483428.1:n.211-1098A=
NM_001242413.2:c.319-1098A=	NP_001229342.1:n.319-1098A=
NM_001282644.1:c.211-1098A=	NP_001269573.1:n.211-1098A=
NM_001282645.1:c.4+2401A=	NP_001269574.1:n.4+2401A=
NM_006257.4:c.319-1098A=	NP_006248.1:n.319-1098A=
XM_005252496.3:c.421-1098A=	XP_005252553.1:n.421-1098A=
XM_005252497.3:c.421-1098A=	XP_005252554.1:n.421-1098A=
XM_006717465.2:c.319-1098A=	XP_006717528.1:n.319-1098A=
XM_011519547.1:c.319-1098A=	XP_011517849.1:n.319-1098A=
XM_011519548.1:c.421-1098A=	XP_011517850.1:n.421-1098A=
NM_001323265.1:c.319-1098A=	NP_001310194.1:n.319-1098A=
NM_001323266.1:c.4+2401A=	NP_001310195.1:n.4+2401A=
NM_001323267.1:c.211-1098A=	NP_001310196.1:n.211-1098A=
XM_005252496.4:c.421-1098A=	XP_005252553.1:n.421-1098A=
XM_005252497.4:c.421-1098A=	XP_005252554.1:n.421-1098A=
XM_024448076.1:c.319-1098A=	XP_024303844.1:n.319-1098A=
XM_024448077.1:c.4+2401A=	XP_024303845.1:n.4+2401A=
NM_001282644.2:c.211-1098A=	NP_001269573.1:n.211-1098A=
NM_001323266.2:c.4+2401A=	NP_001310195.1:n.4+2401A=
NM_006257.5:c.319-1098A= MANE Select	NP_006248.1:n.319-1098A=
NM_001323267.2:c.211-1098A=	NP_001310196.1:n.211-1098A=