Canonical Allele Identifier: CA2339042160
Gene: PRKD2 HGNC NCBI

Linked Data

dbSNP Id: rs2053690583

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46704800dup , CM000681.2:g.46704800dup GRCh38
NC_000019.9:g.47208057dup , CM000681.1:g.47208057dup GRCh37
NC_000019.8:g.51899897dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291281.9:c.512-151dup MANE Select ENSP00000291281.3:n.512-151dup
ENST00000291281.8:c.512-151dup ENSP00000291281.3:n.512-151dup
ENST00000433867.5:c.512-151dup ENSP00000393978.1:n.512-151dup
ENST00000595132.5:c.41-151dup ENSP00000470363.1:n.41-151dup
ENST00000595515.5:c.512-151dup ENSP00000470804.1:n.512-151dup
ENST00000597641.1:c.247-151dup ENSP00000469064.1:n.247-151dup
ENST00000598633.1:c.41-151dup ENSP00000470919.1:n.41-151dup
ENST00000600194.5:c.41-151dup ENSP00000472744.1:n.41-151dup
ENST00000601605.5:c.41-3688dup ENSP00000470442.1:n.41-3688dup
ENST00000601806.5:c.41-151dup ENSP00000469106.1:n.41-151dup
NM_001079880.1:c.512-151dup NP_001073349.1:n.512-151dup
NM_001079881.1:c.512-151dup NP_001073350.1:n.512-151dup
NM_001079882.1:c.41-151dup NP_001073351.1:n.41-151dup
NM_016457.4:c.512-151dup NP_057541.2:n.512-151dup
XM_005258716.2:c.41-151dup XP_005258773.2:n.41-151dup
NM_001079880.2:c.512-151dup NP_001073349.1:n.512-151dup
NM_001079881.2:c.512-151dup NP_001073350.1:n.512-151dup
NM_001079882.2:c.41-151dup NP_001073351.1:n.41-151dup
NM_016457.5:c.512-151dup MANE Select NP_057541.2:n.512-151dup