Canonical Allele Identifier: CA2501310240
Gene: PRKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46704484C>A , CM000681.2:g.46704484C>A GRCh38
NC_000019.9:g.47207741C>A , CM000681.1:g.47207741C>A GRCh37
NC_000019.8:g.51899581C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291281.9:c.666+11G>T MANE Select ENSP00000291281.3:n.666+11G>T
ENST00000291281.8:c.666+11G>T ENSP00000291281.3:n.666+11G>T
ENST00000433867.5:c.666+11G>T ENSP00000393978.1:n.666+11G>T
ENST00000595515.5:c.666+11G>T ENSP00000470804.1:n.666+11G>T
ENST00000597641.1:c.401+11G>T ENSP00000469064.1:n.401+11G>T
ENST00000600194.5:c.195+11G>T ENSP00000472744.1:n.195+11G>T
ENST00000601605.5:c.41-3372G>T ENSP00000470442.1:n.41-3372G>T
ENST00000601806.5:c.195+11G>T ENSP00000469106.1:n.195+11G>T
NM_001079880.1:c.666+11G>T NP_001073349.1:n.666+11G>T
NM_001079881.1:c.666+11G>T NP_001073350.1:n.666+11G>T
NM_001079882.1:c.195+11G>T NP_001073351.1:n.195+11G>T
NM_016457.4:c.666+11G>T NP_057541.2:n.666+11G>T
XM_005258716.2:c.195+11G>T XP_005258773.2:n.195+11G>T
NM_001079880.2:c.666+11G>T NP_001073349.1:n.666+11G>T
NM_001079881.2:c.666+11G>T NP_001073350.1:n.666+11G>T
NM_001079882.2:c.195+11G>T NP_001073351.1:n.195+11G>T
NM_016457.5:c.666+11G>T MANE Select NP_057541.2:n.666+11G>T