Canonical Allele Identifier: CA2533142773
Gene: PRKCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66441832A>T , CM000679.2:g.66441832A>T GRCh38
NC_000017.10:g.64437950A>T , CM000679.1:g.64437950A>T GRCh37
NC_000017.9:g.61868412A>T NCBI36
NG_012206.1:g.144025A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000413366.8:c.206-54369A>T MANE Select ENSP00000408695.3:n.206-54369A>T
ENST00000284384.6:c.198-54369A>T
ENST00000413366.7:c.206-54369A>T ENSP00000408695.3:n.206-54369A>T
ENST00000578063.5:c.206-54369A>T ENSP00000462087.1:n.206-54369A>T
NM_002737.2:c.206-54369A>T NP_002728.1:n.206-54369A>T
XM_011524990.1:c.206-54369A>T XP_011523292.1:n.206-54369A>T
XM_011524991.1:c.206-54369A>T XP_011523293.1:n.206-54369A>T
XM_011524992.1:c.206-54369A>T XP_011523294.1:n.206-54369A>T
XM_017024836.2:c.206-54369A>T XP_016880325.1:n.206-54369A>T
XM_017024841.1:c.206-54369A>T XP_016880330.1:n.206-54369A>T
XR_001752558.1:n.418-54369A>T
NM_002737.3:c.206-54369A>T MANE Select NP_002728.2:n.206-54369A>T