Canonical Allele Identifier: CA16378527

Gene: PRKCQ

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6514592C>T , CM000672.2:g.6514592C>T	GRCh38
NC_000010.10:g.6556554C>T , CM000672.1:g.6556554C>T	GRCh37
NC_000010.9:g.6596560C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263125.10:c.118+426G>A MANE Select	ENSP00000263125.5:n.118+426G>A
ENST00000263125.9:c.118+426G>A	ENSP00000263125.5:n.118+426G>A
ENST00000397176.6:c.118+426G>A	ENSP00000380361.2:n.118+426G>A
ENST00000539722.5:c.-197+426G>A	ENSP00000441752.1:n.-197+426G>A
NM_001242413.2:c.118+426G>A	NP_001229342.1:n.118+426G>A
NM_001282644.1:c.12+426G>A	NP_001269573.1:n.12+426G>A
NM_001282645.1:c.-197+426G>A	NP_001269574.1:n.-197+426G>A
NM_006257.4:c.118+426G>A	NP_006248.1:n.118+426G>A
XM_005252496.3:c.220+426G>A	XP_005252553.1:n.220+426G>A
XM_005252497.3:c.220+426G>A	XP_005252554.1:n.220+426G>A
XM_006717465.2:c.118+426G>A	XP_006717528.1:n.118+426G>A
XM_011519547.1:c.118+426G>A	XP_011517849.1:n.118+426G>A
XM_011519548.1:c.220+426G>A	XP_011517850.1:n.220+426G>A
NM_001323265.1:c.118+426G>A	NP_001310194.1:n.118+426G>A
NM_001323266.1:c.-195+426G>A	NP_001310195.1:n.-195+426G>A
NM_001323267.1:c.12+426G>A	NP_001310196.1:n.12+426G>A
XM_005252496.4:c.220+426G>A	XP_005252553.1:n.220+426G>A
XM_005252497.4:c.220+426G>A	XP_005252554.1:n.220+426G>A
XM_024448076.1:c.118+426G>A	XP_024303844.1:n.118+426G>A
XM_024448077.1:c.-197+426G>A	XP_024303845.1:n.-197+426G>A
NM_001282644.2:c.12+426G>A	NP_001269573.1:n.12+426G>A
NM_001323266.2:c.-195+426G>A	NP_001310195.1:n.-195+426G>A
NM_006257.5:c.118+426G>A MANE Select	NP_006248.1:n.118+426G>A
NM_001323267.2:c.12+426G>A	NP_001310196.1:n.12+426G>A