Canonical Allele Identifier: CA2495062246

Gene: PRKCE

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.45949823C>T , CM000664.2:g.45949823C>T	GRCh38
NC_000002.11:g.46176962C>T , CM000664.1:g.46176962C>T	GRCh37
NC_000002.10:g.46030466C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306156.8:c.413-26606C>T MANE Select	ENSP00000306124.3:n.413-26606C>T
ENST00000306156.7:c.413-26606C>T	ENSP00000306124.3:n.413-26606C>T
ENST00000476675.5:n.315-26606C>T
ENST00000480453.5:n.285-26606C>T
NM_005400.2:c.413-26606C>T	NP_005391.1:n.413-26606C>T
XM_005264428.1:c.413-26606C>T	XP_005264485.1:n.413-26606C>T
XM_005264429.1:c.413-51581C>T	XP_005264486.1:n.413-51581C>T
XM_005264431.2:c.413-26606C>T	XP_005264488.1:n.413-26606C>T
XM_011532970.1:c.125-26606C>T	XP_011531272.1:n.125-26606C>T
XM_011532971.1:c.125-26606C>T	XP_011531273.1:n.125-26606C>T
XM_011532972.1:c.125-26606C>T	XP_011531274.1:n.125-26606C>T
XM_011532973.1:c.125-26606C>T	XP_011531275.1:n.125-26606C>T
XM_011532974.1:c.125-26606C>T	XP_011531276.1:n.125-26606C>T
XM_011532975.1:c.125-26606C>T	XP_011531277.1:n.125-26606C>T
XM_011532976.1:c.125-26606C>T	XP_011531278.1:n.125-26606C>T
XM_011532977.1:c.71-26606C>T	XP_011531279.1:n.71-26606C>T
XM_011532978.1:c.71-26606C>T	XP_011531280.1:n.71-26606C>T
XM_011532979.1:c.68-26606C>T	XP_011531281.1:n.68-26606C>T
XM_011532980.1:c.-38-26606C>T	XP_011531282.1:n.-38-26606C>T
XM_011532981.1:c.-39+12972C>T	XP_011531283.1:n.-39+12972C>T
XR_939695.1:n.1199-26606C>T
XM_005264431.4:c.413-26606C>T	XP_005264488.1:n.413-26606C>T
XM_011532971.3:c.125-26606C>T	XP_011531273.1:n.125-26606C>T
XM_011532975.3:c.125-26606C>T	XP_011531277.1:n.125-26606C>T
XM_011532978.2:c.71-26606C>T	XP_011531280.1:n.71-26606C>T
XM_011532980.3:c.-38-26606C>T	XP_011531282.1:n.-38-26606C>T
XM_011532981.3:c.-39+12972C>T	XP_011531283.1:n.-39+12972C>T
XM_017004486.2:c.125-26606C>T	XP_016859975.1:n.125-26606C>T
XM_017004487.2:c.71-26606C>T	XP_016859976.1:n.71-26606C>T
XM_017004488.2:c.71-26606C>T	XP_016859977.1:n.71-26606C>T
XM_017004489.2:c.-38-26606C>T	XP_016859978.1:n.-38-26606C>T
XM_017004490.2:c.-38-26606C>T	XP_016859979.1:n.-38-26606C>T
XM_017004491.2:c.-38-26606C>T	XP_016859980.1:n.-38-26606C>T
XM_017004492.2:c.413-26606C>T	XP_016859981.1:n.413-26606C>T
XM_024452991.1:c.-38-26606C>T	XP_024308759.1:n.-38-26606C>T
XM_024452992.1:c.-39+12972C>T	XP_024308760.1:n.-39+12972C>T
XR_001738846.2:n.1199-26606C>T
XR_939695.2:n.1199-26606C>T
NM_005400.3:c.413-26606C>T MANE Select	NP_005391.1:n.413-26606C>T