Canonical Allele Identifier: CA406489888

Gene: PRKD2

Linked Data

• MyVariant Identifiers: chr19:g.47207858T>G (hg19) ; chr19:g.46704601T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46704601T>G , CM000681.2:g.46704601T>G	GRCh38
NC_000019.9:g.47207858T>G , CM000681.1:g.47207858T>G	GRCh37
NC_000019.8:g.51899698T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291281.9:c.560A>C MANE Select	ENSP00000291281.3:p.Asn187Thr
ENST00000291281.8:c.560A>C	ENSP00000291281.3:p.Asn187Thr
ENST00000433867.5:c.560A>C	ENSP00000393978.1:p.Asn187Thr
ENST00000595132.5:c.89A>C	ENSP00000470363.1:p.Asn30Thr
ENST00000595515.5:c.560A>C	ENSP00000470804.1:p.Asn187Thr
ENST00000597641.1:c.295A>C	ENSP00000469064.1:n.295A>C
ENST00000600194.5:c.89A>C	ENSP00000472744.1:p.Asn30Thr
ENST00000601605.5:c.41-3489A>C	ENSP00000470442.1:n.41-3489A>C
ENST00000601806.5:c.89A>C	ENSP00000469106.1:p.Asn30Thr
NM_001079880.1:c.560A>C	NP_001073349.1:p.Asn187Thr
NM_001079881.1:c.560A>C	NP_001073350.1:p.Asn187Thr
NM_001079882.1:c.89A>C	NP_001073351.1:p.Asn30Thr
NM_016457.4:c.560A>C	NP_057541.2:p.Asn187Thr
XM_005258716.2:c.89A>C	XP_005258773.2:p.Asn30Thr
NM_001079880.2:c.560A>C	NP_001073349.1:p.Asn187Thr
NM_001079881.2:c.560A>C	NP_001073350.1:p.Asn187Thr
NM_001079882.2:c.89A>C	NP_001073351.1:p.Asn30Thr
NM_016457.5:c.560A>C MANE Select	NP_057541.2:p.Asn187Thr