Canonical Allele Identifier: CA612984864

Gene: PRKD1

Linked Data

• dbSNP Id: rs1360088532
• gnomAD v2: 14-30095595-GTCTTC-G
• gnomAD v3: 14-29626389-GTCTTC-G
• gnomAD v4: 14-29626389-GTCTTC-G
• MyVariant Identifiers: chr14:g.30095596_30095600del (hg19) ; chr14:g.29626390_29626394del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626396_29626400del , CM000676.2:g.29626396_29626400del	GRCh38
NC_000014.8:g.30095602_30095606del , CM000676.1:g.30095602_30095606del	GRCh37
NC_000014.7:g.29165353_29165357del	NCBI36
NG_052879.1:g.306300_306304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1569+90_1569+94del
ENST00000691517.1:n.1082+90_1082+94del
ENST00000331968.11:c.1798+90_1798+94del MANE Select	ENSP00000333568.6:n.1798+90_1798+94del
ENST00000651571.1:c.1610+90_1610+94del	ENSP00000498919.1:n.1610+90_1610+94del
ENST00000651616.1:c.1679+90_1679+94del	ENSP00000498661.1:n.1679+90_1679+94del
ENST00000331968.9:c.1798+90_1798+94del	ENSP00000333568.5:n.1798+90_1798+94del
ENST00000415220.6:c.1822+90_1822+94del	ENSP00000390535.2:n.1822+90_1822+94del
ENST00000616995.4:c.1798+90_1798+94del	ENSP00000482645.1:n.1798+90_1798+94del
NM_002742.2:c.1798+90_1798+94del	NP_002733.2:n.1798+90_1798+94del
XM_005267859.1:c.1822+90_1822+94del	XP_005267916.1:n.1822+90_1822+94del
XM_011536964.1:c.1594+90_1594+94del	XP_011535266.1:n.1594+90_1594+94del
XM_011536965.1:c.1534+90_1534+94del	XP_011535267.1:n.1534+90_1534+94del
XR_943493.1:n.1937+90_1937+94del
NM_001330069.1:c.1822+90_1822+94del	NP_001316998.1:n.1822+90_1822+94del
NM_001348390.1:c.1534+90_1534+94del	NP_001335319.1:n.1534+90_1534+94del
XM_011536965.2:c.1534+90_1534+94del	XP_011535267.1:n.1534+90_1534+94del
XM_017021462.1:c.1303+90_1303+94del	XP_016876951.1:n.1303+90_1303+94del
XR_943493.2:n.2115+90_2115+94del
NM_001330069.2:c.1822+90_1822+94del	NP_001316998.1:n.1822+90_1822+94del
NM_002742.3:c.1798+90_1798+94del MANE Select	NP_002733.2:n.1798+90_1798+94del