Canonical Allele Identifier: CA2141269843

Gene: PRKCH

Linked Data

• dbSNP Id: rs1884561023

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61452541G>A , CM000676.2:g.61452541G>A	GRCh38
NC_000014.8:g.61919259G>A , CM000676.1:g.61919259G>A	GRCh37
NC_000014.7:g.60989012G>A	NCBI36
NG_011514.1:g.135745G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000332981.11:c.833-685G>A MANE Select	ENSP00000329127.5:n.833-685G>A
ENST00000332981.10:c.833-685G>A	ENSP00000329127.5:n.833-685G>A
ENST00000332981.9:c.833-685G>A	ENSP00000329127.5:n.833-685G>A
ENST00000553726.5:c.26-685G>A	ENSP00000451793.1:n.26-685G>A
ENST00000555082.5:c.350-685G>A	ENSP00000450981.1:n.350-685G>A
ENST00000555185.5:c.-18-32961G>A	ENSP00000451871.1:n.-18-32961G>A
ENST00000556778.5:c.350-685G>A	ENSP00000452055.1:n.350-685G>A
ENST00000557585.5:c.350-685G>A	ENSP00000451930.1:n.350-685G>A
NM_006255.4:c.833-685G>A	NP_006246.2:n.833-685G>A
XM_011536954.1:c.596-685G>A	XP_011535256.1:n.596-685G>A
XM_011536955.1:c.593-685G>A	XP_011535257.1:n.593-685G>A
XM_011536956.1:c.833-685G>A	XP_011535258.1:n.833-685G>A
XM_011536957.1:c.833-685G>A	XP_011535259.1:n.833-685G>A
XM_011536954.3:c.596-685G>A	XP_011535256.1:n.596-685G>A
XM_017021458.1:c.350-685G>A	XP_016876947.1:n.350-685G>A
XM_017021459.1:c.833-685G>A	XP_016876948.1:n.833-685G>A
XM_024449661.1:c.350-685G>A	XP_024305429.1:n.350-685G>A
XM_024449662.1:c.350-685G>A	XP_024305430.1:n.350-685G>A
NM_006255.5:c.833-685G>A MANE Select	NP_006246.2:n.833-685G>A