Canonical Allele Identifier: CA7215551

Gene: PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61549772A>G , CM000676.2:g.61549772A>G	GRCh38
NC_000014.8:g.62016490A>G , CM000676.1:g.62016490A>G	GRCh37
NC_000014.7:g.61086243A>G	NCBI36
NG_011514.1:g.232976A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.1993A>G MANE Select	ENSP00000329127.5:p.Met665Val
ENST00000332981.10:c.1993A>G	ENSP00000329127.5:p.Met665Val
ENST00000332981.9:c.1993A>G	ENSP00000329127.5:p.Met665Val
ENST00000536400.5:n.794A>G
ENST00000555082.5:c.1510A>G	ENSP00000450981.1:p.Met504Val
ENST00000556245.1:n.1545A>G
ENST00000556347.1:c.419+1886A>G
ENST00000557599.5:n.716A>G
NM_006255.4:c.1993A>G	NP_006246.2:p.Met665Val
XM_011536954.1:c.1756A>G	XP_011535256.1:p.Met586Val
XM_011536955.1:c.1753A>G	XP_011535257.1:p.Met585Val
XM_011536954.3:c.1756A>G	XP_011535256.1:p.Met586Val
XM_017021458.1:c.1510A>G	XP_016876947.1:p.Met504Val
XM_024449661.1:c.1510A>G	XP_024305429.1:p.Met504Val
XM_024449662.1:c.1510A>G	XP_024305430.1:p.Met504Val
NM_006255.5:c.1993A>G MANE Select	NP_006246.2:p.Met665Val