Canonical Allele Identifier: CA2126414921

Gene: PRKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.29626471_29626473delinsTGA , CM000676.2:g.29626471_29626473delinsTGA	GRCh38
NC_000014.8:g.30095677_30095679delinsTGA , CM000676.1:g.30095677_30095679delinsTGA	GRCh37
NC_000014.7:g.29165428_29165430delinsTGA	NCBI36
NG_052879.1:g.306221_306223delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616995.5:n.1569+11_1569+13delinsTCA
ENST00000691517.1:n.1082+11_1082+13delinsTCA
ENST00000331968.11:c.1798+11_1798+13delinsTCA MANE Select	ENSP00000333568.6:n.1798+11_1798+13delinsTCA
ENST00000651571.1:c.1610+11_1610+13delinsTCA	ENSP00000498919.1:n.1610+11_1610+13delinsTCA
ENST00000651616.1:c.1679+11_1679+13delinsTCA	ENSP00000498661.1:n.1679+11_1679+13delinsTCA
ENST00000331968.9:c.1798+11_1798+13delinsTCA	ENSP00000333568.5:n.1798+11_1798+13delinsTCA
ENST00000415220.6:c.1822+11_1822+13delinsTCA	ENSP00000390535.2:n.1822+11_1822+13delinsTCA
ENST00000616995.4:c.1798+11_1798+13delinsTCA	ENSP00000482645.1:n.1798+11_1798+13delinsTCA
NM_002742.2:c.1798+11_1798+13delinsTCA	NP_002733.2:n.1798+11_1798+13delinsTCA
XM_005267859.1:c.1822+11_1822+13delinsTCA	XP_005267916.1:n.1822+11_1822+13delinsTCA
XM_011536964.1:c.1594+11_1594+13delinsTCA	XP_011535266.1:n.1594+11_1594+13delinsTCA
XM_011536965.1:c.1534+11_1534+13delinsTCA	XP_011535267.1:n.1534+11_1534+13delinsTCA
XR_943493.1:n.1937+11_1937+13delinsTCA
NM_001330069.1:c.1822+11_1822+13delinsTCA	NP_001316998.1:n.1822+11_1822+13delinsTCA
NM_001348390.1:c.1534+11_1534+13delinsTCA	NP_001335319.1:n.1534+11_1534+13delinsTCA
XM_011536965.2:c.1534+11_1534+13delinsTCA	XP_011535267.1:n.1534+11_1534+13delinsTCA
XM_017021462.1:c.1303+11_1303+13delinsTCA	XP_016876951.1:n.1303+11_1303+13delinsTCA
XR_943493.2:n.2115+11_2115+13delinsTCA
NM_001330069.2:c.1822+11_1822+13delinsTCA	NP_001316998.1:n.1822+11_1822+13delinsTCA
NM_002742.3:c.1798+11_1798+13delinsTCA MANE Select	NP_002733.2:n.1798+11_1798+13delinsTCA