Canonical Allele Identifier: CA15891774

Gene: PRKCA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66521195T>A , CM000679.2:g.66521195T>A	GRCh38
NC_000017.10:g.64517313T>A , CM000679.1:g.64517313T>A	GRCh37
NC_000017.9:g.61947775T>A	NCBI36
NG_012206.1:g.223388T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413366.8:c.288+24912T>A MANE Select	ENSP00000408695.3:n.288+24912T>A
ENST00000284384.6:c.280+24912T>A
ENST00000413366.7:c.288+24912T>A	ENSP00000408695.3:n.288+24912T>A
ENST00000578063.5:c.288+24912T>A	ENSP00000462087.1:n.288+24912T>A
NM_002737.2:c.288+24912T>A	NP_002728.1:n.288+24912T>A
XM_011524989.1:c.30+6729T>A	XP_011523291.1:n.30+6729T>A
XM_011524990.1:c.288+24912T>A	XP_011523292.1:n.288+24912T>A
XM_011524991.1:c.288+24912T>A	XP_011523293.1:n.288+24912T>A
XM_011524992.1:c.288+24912T>A	XP_011523294.1:n.288+24912T>A
XM_017024836.2:c.288+24912T>A	XP_016880325.1:n.288+24912T>A
XM_017024837.1:c.135+24912T>A	XP_016880326.1:n.135+24912T>A
XM_017024841.1:c.288+24912T>A	XP_016880330.1:n.288+24912T>A
XM_024450829.1:c.30+6729T>A	XP_024306597.1:n.30+6729T>A
XM_024450830.1:c.30+6729T>A	XP_024306598.1:n.30+6729T>A
XR_001752558.1:n.500+24912T>A
NM_002737.3:c.288+24912T>A MANE Select	NP_002728.2:n.288+24912T>A