Canonical Allele Identifier: CA293510276

Gene: PRKCA

Linked Data

• dbSNP Id: rs915778197
• MyVariant Identifiers: chr17:g.64438058G>A (hg19) ; chr17:g.66441940G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66441940G>A , CM000679.2:g.66441940G>A	GRCh38
NC_000017.10:g.64438058G>A , CM000679.1:g.64438058G>A	GRCh37
NC_000017.9:g.61868520G>A	NCBI36
NG_012206.1:g.144133G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000413366.8:c.206-54261G>A MANE Select	ENSP00000408695.3:n.206-54261G>A
ENST00000284384.6:c.198-54261G>A
ENST00000413366.7:c.206-54261G>A	ENSP00000408695.3:n.206-54261G>A
ENST00000578063.5:c.206-54261G>A	ENSP00000462087.1:n.206-54261G>A
NM_002737.2:c.206-54261G>A	NP_002728.1:n.206-54261G>A
XM_011524990.1:c.206-54261G>A	XP_011523292.1:n.206-54261G>A
XM_011524991.1:c.206-54261G>A	XP_011523293.1:n.206-54261G>A
XM_011524992.1:c.206-54261G>A	XP_011523294.1:n.206-54261G>A
XM_017024836.2:c.206-54261G>A	XP_016880325.1:n.206-54261G>A
XM_017024841.1:c.206-54261G>A	XP_016880330.1:n.206-54261G>A
XR_001752558.1:n.418-54261G>A
NM_002737.3:c.206-54261G>A MANE Select	NP_002728.2:n.206-54261G>A