Canonical Allele Identifier: CA261734703

Gene: PRKCH

Linked Data

• dbSNP Id: rs554886977
• gnomAD v3: 14-61452631-A-C
• gnomAD v4: 14-61452631-A-C
• MyVariant Identifiers: chr14:g.61919349A>C (hg19) ; chr14:g.61452631A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61452631A>C , CM000676.2:g.61452631A>C	GRCh38
NC_000014.8:g.61919349A>C , CM000676.1:g.61919349A>C	GRCh37
NC_000014.7:g.60989102A>C	NCBI36
NG_011514.1:g.135835A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332981.11:c.833-595A>C MANE Select	ENSP00000329127.5:n.833-595A>C
ENST00000332981.10:c.833-595A>C	ENSP00000329127.5:n.833-595A>C
ENST00000332981.9:c.833-595A>C	ENSP00000329127.5:n.833-595A>C
ENST00000553726.5:c.26-595A>C	ENSP00000451793.1:n.26-595A>C
ENST00000555082.5:c.350-595A>C	ENSP00000450981.1:n.350-595A>C
ENST00000555185.5:c.-18-32871A>C	ENSP00000451871.1:n.-18-32871A>C
ENST00000556778.5:c.350-595A>C	ENSP00000452055.1:n.350-595A>C
ENST00000557585.5:c.350-595A>C	ENSP00000451930.1:n.350-595A>C
NM_006255.4:c.833-595A>C	NP_006246.2:n.833-595A>C
XM_011536954.1:c.596-595A>C	XP_011535256.1:n.596-595A>C
XM_011536955.1:c.593-595A>C	XP_011535257.1:n.593-595A>C
XM_011536956.1:c.833-595A>C	XP_011535258.1:n.833-595A>C
XM_011536957.1:c.833-595A>C	XP_011535259.1:n.833-595A>C
XM_011536954.3:c.596-595A>C	XP_011535256.1:n.596-595A>C
XM_017021458.1:c.350-595A>C	XP_016876947.1:n.350-595A>C
XM_017021459.1:c.833-595A>C	XP_016876948.1:n.833-595A>C
XM_024449661.1:c.350-595A>C	XP_024305429.1:n.350-595A>C
XM_024449662.1:c.350-595A>C	XP_024305430.1:n.350-595A>C
NM_006255.5:c.833-595A>C MANE Select	NP_006246.2:n.833-595A>C