Canonical Allele Identifier: CA507877031

Gene: PRKD2

Linked Data

• MyVariant Identifiers: chr19:g.47207857G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46704600G>A , CM000681.2:g.46704600G>A	GRCh38
NC_000019.9:g.47207857G>A , CM000681.1:g.47207857G>A	GRCh37
NC_000019.8:g.51899697G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291281.9:c.561C>T MANE Select	ENSP00000291281.3:p.Asn187=
ENST00000291281.8:c.561C>T	ENSP00000291281.3:p.Asn187=
ENST00000433867.5:c.561C>T	ENSP00000393978.1:p.Asn187=
ENST00000595132.5:c.90C>T	ENSP00000470363.1:p.Asn30=
ENST00000595515.5:c.561C>T	ENSP00000470804.1:p.Asn187=
ENST00000597641.1:c.296C>T	ENSP00000469064.1:n.296C>T
ENST00000600194.5:c.90C>T	ENSP00000472744.1:p.Asn30=
ENST00000601605.5:c.41-3488C>T	ENSP00000470442.1:n.41-3488C>T
ENST00000601806.5:c.90C>T	ENSP00000469106.1:p.Asn30=
NM_001079880.1:c.561C>T	NP_001073349.1:p.Asn187=
NM_001079881.1:c.561C>T	NP_001073350.1:p.Asn187=
NM_001079882.1:c.90C>T	NP_001073351.1:p.Asn30=
NM_016457.4:c.561C>T	NP_057541.2:p.Asn187=
XM_005258716.2:c.90C>T	XP_005258773.2:p.Asn30=
NM_001079880.2:c.561C>T	NP_001073349.1:p.Asn187=
NM_001079881.2:c.561C>T	NP_001073350.1:p.Asn187=
NM_001079882.2:c.90C>T	NP_001073351.1:p.Asn30=
NM_016457.5:c.561C>T MANE Select	NP_057541.2:p.Asn187=