Canonical Allele Identifier: CA2581320779
Community Standard Title: NM_002737.3(PRKCA):c.1606-3555G>A
Gene: PRKCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66783312G>A , CM000679.2:g.66783312G>A GRCh38
NC_000017.10:g.64779430G>A , CM000679.1:g.64779430G>A GRCh37
NC_000017.9:g.62209892G>A NCBI36
NG_012206.1:g.485505G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002737.3:c.1606-3555G>A MANE Select NP_002728.2:n.1606-3555G>A
ENST00000413366.8:c.1606-3555G>A MANE Select ENSP00000408695.3:n.1606-3555G>A
NM_002737.2:c.1606-3555G>A NP_002728.1:n.1606-3555G>A
ENST00000413366.7:c.1606-3555G>A ENSP00000408695.3:n.1606-3555G>A
XM_011524989.1:c.1348-3555G>A XP_011523291.1:n.1348-3555G>A
XM_011524990.1:c.1606-3555G>A XP_011523292.1:n.1606-3555G>A
XM_017024836.2:c.1606-3555G>A XP_016880325.1:n.1606-3555G>A
XM_017024837.1:c.1453-3555G>A XP_016880326.1:n.1453-3555G>A
XM_024450829.1:c.1348-3555G>A XP_024306597.1:n.1348-3555G>A
XM_024450830.1:c.1348-3555G>A XP_024306598.1:n.1348-3555G>A