Canonical Allele Identifier: CA2624426561
Gene: PRKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.29626410C>A , CM000676.2:g.29626410C>A GRCh38
NC_000014.8:g.30095616C>A , CM000676.1:g.30095616C>A GRCh37
NC_000014.7:g.29165367C>A NCBI36
NG_052879.1:g.306284G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000616995.5:n.1569+74G>T
ENST00000691517.1:n.1082+74G>T
ENST00000331968.11:c.1798+74G>T MANE Select ENSP00000333568.6:n.1798+74G>T
ENST00000651571.1:c.1610+74G>T ENSP00000498919.1:n.1610+74G>T
ENST00000651616.1:c.1679+74G>T ENSP00000498661.1:n.1679+74G>T
ENST00000331968.9:c.1798+74G>T ENSP00000333568.5:n.1798+74G>T
ENST00000415220.6:c.1822+74G>T ENSP00000390535.2:n.1822+74G>T
ENST00000616995.4:c.1798+74G>T ENSP00000482645.1:n.1798+74G>T
NM_002742.2:c.1798+74G>T NP_002733.2:n.1798+74G>T
XM_005267859.1:c.1822+74G>T XP_005267916.1:n.1822+74G>T
XM_011536964.1:c.1594+74G>T XP_011535266.1:n.1594+74G>T
XM_011536965.1:c.1534+74G>T XP_011535267.1:n.1534+74G>T
XR_943493.1:n.1937+74G>T
NM_001330069.1:c.1822+74G>T NP_001316998.1:n.1822+74G>T
NM_001348390.1:c.1534+74G>T NP_001335319.1:n.1534+74G>T
XM_011536965.2:c.1534+74G>T XP_011535267.1:n.1534+74G>T
XM_017021462.1:c.1303+74G>T XP_016876951.1:n.1303+74G>T
XR_943493.2:n.2115+74G>T
NM_001330069.2:c.1822+74G>T NP_001316998.1:n.1822+74G>T
NM_002742.3:c.1798+74G>T MANE Select NP_002733.2:n.1798+74G>T