Canonical Allele Identifier: CA14408520
Gene: PRKCA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1005651

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66441893C>A , CM000679.2:g.66441893C>A GRCh38
NC_000017.10:g.64438011C>A , CM000679.1:g.64438011C>A GRCh37
NC_000017.9:g.61868473C>A NCBI36
NG_012206.1:g.144086C>A

Transcript Alleles

HGVS Amino-acid change
NM_002737.2:c.206-54308C>A VV NP_002728.1:p.=
XM_011524990.1:c.206-54308C>A XP_011523292.1:p.=
XM_011524991.1:c.206-54308C>A XP_011523293.1:p.=
XM_011524992.1:c.206-54308C>A XP_011523294.1:p.=
XM_017024836.2:c.206-54308C>A XP_016880325.1:p.=
XM_017024841.1:c.206-54308C>A XP_016880330.1:p.=
XR_001752558.1:n.418-54308C>A
NM_002737.3:c.206-54308C>A VV MANE Preferred NP_002728.2:p.=
ENST00000284384.6:n.198-54308C>A
ENST00000413366.7:c.206-54308C>A ENSP00000408695.3:p.=
ENST00000578063.5:c.206-54308C>A ENSP00000462087.1:p.=