Canonical Allele Identifier: CA2739306244

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61452498C>G , CM000676.2:g.61452498C>G	GRCh38
NC_000014.8:g.61919216C>G , CM000676.1:g.61919216C>G	GRCh37
NC_000014.7:g.60988969C>G	NCBI36
NG_011514.1:g.135702C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006255.5:c.833-728C>G MANE Select	NP_006246.2:n.833-728C>G
ENST00000332981.11:c.833-728C>G MANE Select	ENSP00000329127.5:n.833-728C>G
NM_006255.4:c.833-728C>G	NP_006246.2:n.833-728C>G
ENST00000332981.10:c.833-728C>G	ENSP00000329127.5:n.833-728C>G
ENST00000332981.9:c.833-728C>G	ENSP00000329127.5:n.833-728C>G
ENST00000553726.5:c.26-728C>G	ENSP00000451793.1:n.26-728C>G
ENST00000555082.5:c.350-728C>G	ENSP00000450981.1:n.350-728C>G
ENST00000555185.5:c.-18-33004C>G	ENSP00000451871.1:n.-18-33004C>G
ENST00000556778.5:c.350-728C>G	ENSP00000452055.1:n.350-728C>G
ENST00000557585.5:c.350-728C>G	ENSP00000451930.1:n.350-728C>G
XM_011536954.1:c.596-728C>G	XP_011535256.1:n.596-728C>G
XM_011536954.3:c.596-728C>G	XP_011535256.1:n.596-728C>G
XM_011536955.1:c.593-728C>G	XP_011535257.1:n.593-728C>G
XM_011536956.1:c.833-728C>G	XP_011535258.1:n.833-728C>G
XM_011536957.1:c.833-728C>G	XP_011535259.1:n.833-728C>G
XM_017021458.1:c.350-728C>G	XP_016876947.1:n.350-728C>G
XM_017021459.1:c.833-728C>G	XP_016876948.1:n.833-728C>G
XM_024449661.1:c.350-728C>G	XP_024305429.1:n.350-728C>G
XM_024449662.1:c.350-728C>G	XP_024305430.1:n.350-728C>G