Canonical Allele Identifier: CA532506681

Gene: PRKCE

Linked Data

• dbSNP Id: rs1188962104
• gnomAD v2: 2-46321107-G-T
• gnomAD v3: 2-46093968-G-T
• gnomAD v4: 2-46093968-G-T
• MyVariant Identifiers: chr2:g.46321107G>T (hg19) ; chr2:g.46093968G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46093968G>T , CM000664.2:g.46093968G>T	GRCh38
NC_000002.11:g.46321107G>T , CM000664.1:g.46321107G>T	GRCh37
NC_000002.10:g.46174611G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306156.8:c.1592+7606G>T MANE Select	ENSP00000306124.3:n.1592+7606G>T
ENST00000306156.7:c.1592+7606G>T	ENSP00000306124.3:n.1592+7606G>T
ENST00000469753.5:n.679+7606G>T
ENST00000480633.1:n.358+7606G>T
NM_005400.2:c.1592+7606G>T	NP_005391.1:n.1592+7606G>T
XM_005264428.1:c.1592+7606G>T	XP_005264485.1:n.1592+7606G>T
XM_005264429.1:c.1181+7606G>T	XP_005264486.1:n.1181+7606G>T
XM_006712050.2:c.761+7606G>T	XP_006712113.1:n.761+7606G>T
XM_011532970.1:c.1304+7606G>T	XP_011531272.1:n.1304+7606G>T
XM_011532971.1:c.1304+7606G>T	XP_011531273.1:n.1304+7606G>T
XM_011532972.1:c.1304+7606G>T	XP_011531274.1:n.1304+7606G>T
XM_011532973.1:c.1304+7606G>T	XP_011531275.1:n.1304+7606G>T
XM_011532974.1:c.1304+7606G>T	XP_011531276.1:n.1304+7606G>T
XM_011532975.1:c.1304+7606G>T	XP_011531277.1:n.1304+7606G>T
XM_011532976.1:c.1304+7606G>T	XP_011531278.1:n.1304+7606G>T
XM_011532977.1:c.1250+7606G>T	XP_011531279.1:n.1250+7606G>T
XM_011532978.1:c.1250+7606G>T	XP_011531280.1:n.1250+7606G>T
XM_011532979.1:c.1247+7606G>T	XP_011531281.1:n.1247+7606G>T
XM_011532980.1:c.1142+7606G>T	XP_011531282.1:n.1142+7606G>T
XM_011532981.1:c.1142+7606G>T	XP_011531283.1:n.1142+7606G>T
XM_011532982.1:c.872+7606G>T	XP_011531284.1:n.872+7606G>T
XM_011532983.1:c.689+7606G>T	XP_011531285.1:n.689+7606G>T
XM_006712050.3:c.761+7606G>T	XP_006712113.1:n.761+7606G>T
XM_011532971.3:c.1304+7606G>T	XP_011531273.1:n.1304+7606G>T
XM_011532975.3:c.1304+7606G>T	XP_011531277.1:n.1304+7606G>T
XM_011532978.2:c.1250+7606G>T	XP_011531280.1:n.1250+7606G>T
XM_011532980.3:c.1142+7606G>T	XP_011531282.1:n.1142+7606G>T
XM_011532981.3:c.1142+7606G>T	XP_011531283.1:n.1142+7606G>T
XM_011532982.2:c.872+7606G>T	XP_011531284.1:n.872+7606G>T
XM_011532983.2:c.689+7606G>T	XP_011531285.1:n.689+7606G>T
XM_017004486.2:c.1304+7606G>T	XP_016859975.1:n.1304+7606G>T
XM_017004487.2:c.1250+7606G>T	XP_016859976.1:n.1250+7606G>T
XM_017004488.2:c.1250+7606G>T	XP_016859977.1:n.1250+7606G>T
XM_017004489.2:c.1142+7606G>T	XP_016859978.1:n.1142+7606G>T
XM_017004490.2:c.1142+7606G>T	XP_016859979.1:n.1142+7606G>T
XM_017004491.2:c.1142+7606G>T	XP_016859980.1:n.1142+7606G>T
XM_024452991.1:c.1142+7606G>T	XP_024308759.1:n.1142+7606G>T
XM_024452992.1:c.1142+7606G>T	XP_024308760.1:n.1142+7606G>T
NM_005400.3:c.1592+7606G>T MANE Select	NP_005391.1:n.1592+7606G>T