Canonical Allele Identifier: CA257951429

Gene: PRKD1

Linked Data

• dbSNP Id: rs766771709
• MyVariant Identifiers: chr14:g.30095534_30095535insA (hg19) ; chr14:g.29626328_29626329insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626335dup , CM000676.2:g.29626335dup	GRCh38
NC_000014.8:g.30095541dup , CM000676.1:g.30095541dup	GRCh37
NC_000014.7:g.29165292dup	NCBI36
NG_052879.1:g.306365dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1569+155dup
ENST00000691517.1:n.1082+155dup
ENST00000331968.11:c.1798+155dup MANE Select	ENSP00000333568.6:n.1798+155dup
ENST00000651571.1:c.1610+155dup	ENSP00000498919.1:n.1610+155dup
ENST00000651616.1:c.1679+155dup	ENSP00000498661.1:n.1679+155dup
ENST00000331968.9:c.1798+155dup	ENSP00000333568.5:n.1798+155dup
ENST00000415220.6:c.1822+155dup	ENSP00000390535.2:n.1822+155dup
ENST00000616995.4:c.1798+155dup	ENSP00000482645.1:n.1798+155dup
NM_002742.2:c.1798+155dup	NP_002733.2:n.1798+155dup
XM_005267859.1:c.1822+155dup	XP_005267916.1:n.1822+155dup
XM_011536964.1:c.1594+155dup	XP_011535266.1:n.1594+155dup
XM_011536965.1:c.1534+155dup	XP_011535267.1:n.1534+155dup
XR_943493.1:n.1937+155dup
NM_001330069.1:c.1822+155dup	NP_001316998.1:n.1822+155dup
NM_001348390.1:c.1534+155dup	NP_001335319.1:n.1534+155dup
XM_011536965.2:c.1534+155dup	XP_011535267.1:n.1534+155dup
XM_017021462.1:c.1303+155dup	XP_016876951.1:n.1303+155dup
XR_943493.2:n.2115+155dup
NM_001330069.2:c.1822+155dup	NP_001316998.1:n.1822+155dup
NM_002742.3:c.1798+155dup MANE Select	NP_002733.2:n.1798+155dup