Canonical Allele Identifier: CA14500442
Gene: PRKCA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66796013G>A , CM000679.2:g.66796013G>A GRCh38
NC_000017.10:g.64792131G>A , CM000679.1:g.64792131G>A GRCh37
NC_000017.9:g.62222593G>A NCBI36
NG_012206.1:g.498206G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000413366.8:c.1854+7034G>A MANE Select ENSP00000408695.3:n.1854+7034G>A
ENST00000413366.7:c.1854+7034G>A ENSP00000408695.3:n.1854+7034G>A
NM_002737.2:c.1854+7034G>A NP_002728.1:n.1854+7034G>A
XM_011524989.1:c.1597-435G>A XP_011523291.1:n.1597-435G>A
XM_011524990.1:c.1855-435G>A XP_011523292.1:n.1855-435G>A
XM_017024836.2:c.1855-435G>A XP_016880325.1:n.1855-435G>A
XM_017024837.1:c.1701+7034G>A XP_016880326.1:n.1701+7034G>A
XM_024450829.1:c.1596+7034G>A XP_024306597.1:n.1596+7034G>A
XM_024450830.1:c.1596+7034G>A XP_024306598.1:n.1596+7034G>A
NM_002737.3:c.1854+7034G>A MANE Select NP_002728.2:n.1854+7034G>A
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