Canonical Allele Identifier: CA15825295
Gene: PRKCH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1957895

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.61441614G>T , CM000676.2:g.61441614G>T GRCh38
NC_000014.7:g.60978085G>T NCBI36
NC_000014.8:g.61908332G>T , CM000676.1:g.61908332G>T GRCh37
NG_011514.1:g.124818G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000332981.9:c.428-1497G>T ENSP00000329127.5:p.=
ENST00000553265.5:c.-56-1497G>T ENSP00000451933.1:p.=
ENST00000553726.5:c.-229-4078G>T ENSP00000451793.1:p.=
ENST00000553830.1:c.254-1497G>T ENSP00000452588.1:p.=
ENST00000553831.5:c.-56-1497G>T ENSP00000450959.1:p.=
ENST00000555082.5:c.-56-1497G>T ENSP00000450981.1:p.=
ENST00000555185.5:c.-18-43888G>T ENSP00000451871.1:p.=
ENST00000555542.5:c.-56-1497G>T ENSP00000451789.1:p.=
ENST00000555906.5:c.-56-1497G>T ENSP00000451205.1:p.=
ENST00000556164.5:c.-56-1497G>T ENSP00000452330.1:p.=
ENST00000556778.5:c.-56-1497G>T ENSP00000452055.1:p.=
ENST00000557585.5:c.-56-1497G>T ENSP00000451930.1:p.=
NM_006255.4:c.428-1497G>T VV NP_006246.2:p.=
XM_011536954.1:c.191-1497G>T XP_011535256.1:p.=
XM_011536955.1:c.188-1497G>T XP_011535257.1:p.=
XM_011536956.1:c.428-1497G>T XP_011535258.1:p.=
XM_011536957.1:c.428-1497G>T XP_011535259.1:p.=
XM_011536954.3:c.191-1497G>T
XM_017021458.1:c.-56-1497G>T XP_016876947.1:p.=
XM_017021459.1:c.428-1497G>T XP_016876948.1:p.=
XM_024449661.1:c.-56-1497G>T XP_024305429.1:p.=
XM_024449662.1:c.-56-1497G>T XP_024305430.1:p.=