Canonical Allele Identifier: CA1322803571
Gene: PARD3B HGNC NCBI

Linked Data

dbSNP Id: rs2041373510

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.205285800_205285801del , CM000664.2:g.205285800_205285801del GRCh38
NC_000002.11:g.206150524_206150525del , CM000664.1:g.206150524_206150525del GRCh37
NC_000002.10:g.205858769_205858770del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406610.7:c.2186-14730_2186-14729del MANE Select ENSP00000385848.2:n.2186-14730_2186-14729...
ENST00000349953.7:c.2186-14730_2186-14729del ENSP00000340280.3:n.2186-14730_2186-14729...
ENST00000351153.5:c.2186-15664_2186-15663del ENSP00000317261.2:n.2186-15664_2186-15663...
ENST00000358768.6:c.2000-14730_2000-14729del ENSP00000351618.2:n.2000-14730_2000-14729...
ENST00000406610.6:c.2186-14730_2186-14729del ENSP00000385848.2:n.2186-14730_2186-14729...
ENST00000462231.5:c.2186-14730_2186-14729del ENSP00000473503.1:n.2186-14730_2186-14729...
ENST00000613457.4:c.1778-14730_1778-14729del ENSP00000484434.1:n.1778-14730_1778-14729...
ENST00000614500.3:c.1964-15664_1964-15663del ENSP00000481918.1:n.1964-15664_1964-15663...
ENST00000622699.2:c.1964-14730_1964-14729del ENSP00000482649.1:n.1964-14730_1964-14729...
NM_001302769.1:c.2186-14730_2186-14729del NP_001289698.1:n.2186-14730_2186-14729del...
NM_057177.6:c.2186-15664_2186-15663del NP_476518.4:n.2186-15664_2186-15663del
NM_152526.5:c.2000-14730_2000-14729del NP_689739.4:n.2000-14730_2000-14729del
NM_205863.3:c.2186-14730_2186-14729del NP_995585.2:n.2186-14730_2186-14729del
XM_011510550.1:c.2186-14730_2186-14729del XP_011508852.1:n.2186-14730_2186-14729del...
XM_011510551.1:c.2186-14730_2186-14729del XP_011508853.1:n.2186-14730_2186-14729del...
XM_011510552.1:c.2210-14730_2210-14729del XP_011508854.1:n.2210-14730_2210-14729del...
XM_011510553.1:c.2210-14730_2210-14729del XP_011508855.1:n.2210-14730_2210-14729del...
XM_011510552.2:c.2210-14730_2210-14729del XP_011508854.1:n.2210-14730_2210-14729del...
XM_011510553.2:c.2210-14730_2210-14729del XP_011508855.1:n.2210-14730_2210-14729del...
XM_017003283.1:c.2150-14730_2150-14729del XP_016858772.1:n.2150-14730_2150-14729del...
XM_017003284.1:c.2120-14730_2120-14729del XP_016858773.1:n.2120-14730_2120-14729del...
XM_017003285.1:c.2024-14730_2024-14729del XP_016858774.1:n.2024-14730_2024-14729del...
XM_017003286.1:c.2018-14730_2018-14729del XP_016858775.1:n.2018-14730_2018-14729del...
XM_017003287.1:c.2210-14730_2210-14729del XP_016858776.1:n.2210-14730_2210-14729del...
XM_017003288.1:c.2210-14730_2210-14729del XP_016858777.1:n.2210-14730_2210-14729del...
XM_017003289.1:c.1685-14730_1685-14729del XP_016858778.1:n.1685-14730_1685-14729del...
XM_017003290.1:c.1589-14730_1589-14729del XP_016858779.1:n.1589-14730_1589-14729del...
XM_017003291.1:c.1589-14730_1589-14729del XP_016858780.1:n.1589-14730_1589-14729del...
XM_017003292.1:c.1589-14730_1589-14729del XP_016858781.1:n.1589-14730_1589-14729del...
XM_017003293.1:c.1589-14730_1589-14729del XP_016858782.1:n.1589-14730_1589-14729del...
NM_001302769.2:c.2186-14730_2186-14729del MANE Select NP_001289698.1:n.2186-14730_2186-14729del...
NM_057177.7:c.2186-15664_2186-15663del NP_476518.4:n.2186-15664_2186-15663del
NM_152526.6:c.2000-14730_2000-14729del NP_689739.4:n.2000-14730_2000-14729del
NM_205863.4:c.2186-14730_2186-14729del NP_995585.2:n.2186-14730_2186-14729del