Canonical Allele Identifier: CA262251818

Gene: PRKCH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61267922T>A , CM000676.2:g.61267922T>A	GRCh38
NC_000014.8:g.61734640T>A , CM000676.1:g.61734640T>A	GRCh37
NC_000014.7:g.60804393T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555185.5:c.-19+80254T>A	ENSP00000451871.1:n.-19+80254T>A
ENST00000556778.5:c.-57+80254T>A	ENSP00000452055.1:n.-57+80254T>A
ENST00000557294.5:c.-108-54072T>A	ENSP00000452129.1:n.-108-54072T>A
XM_024449661.1:c.-121+80254T>A	XP_024305429.1:n.-121+80254T>A