Canonical Allele Identifier: CA916757987

Gene: PARD3B

Linked Data

• dbSNP Id: rs1574598509
• gnomAD v3: 2-205285839-TGA-T
• gnomAD v4: 2-205285839-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.205285843_205285844del , CM000664.2:g.205285843_205285844del	GRCh38
NC_000002.11:g.206150567_206150568del , CM000664.1:g.206150567_206150568del	GRCh37
NC_000002.10:g.205858812_205858813del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406610.7:c.2186-14687_2186-14686del MANE Select	ENSP00000385848.2:n.2186-14687_2186-14686del
ENST00000349953.7:c.2186-14687_2186-14686del	ENSP00000340280.3:n.2186-14687_2186-14686del
ENST00000351153.5:c.2186-15621_2186-15620del	ENSP00000317261.2:n.2186-15621_2186-15620del
ENST00000358768.6:c.2000-14687_2000-14686del	ENSP00000351618.2:n.2000-14687_2000-14686del
ENST00000406610.6:c.2186-14687_2186-14686del	ENSP00000385848.2:n.2186-14687_2186-14686del
ENST00000462231.5:c.2186-14687_2186-14686del	ENSP00000473503.1:n.2186-14687_2186-14686del
ENST00000613457.4:c.1778-14687_1778-14686del	ENSP00000484434.1:n.1778-14687_1778-14686del
ENST00000614500.3:c.1964-15621_1964-15620del	ENSP00000481918.1:n.1964-15621_1964-15620del
ENST00000622699.2:c.1964-14687_1964-14686del	ENSP00000482649.1:n.1964-14687_1964-14686del
NM_001302769.1:c.2186-14687_2186-14686del	NP_001289698.1:n.2186-14687_2186-14686del
NM_057177.6:c.2186-15621_2186-15620del	NP_476518.4:n.2186-15621_2186-15620del
NM_152526.5:c.2000-14687_2000-14686del	NP_689739.4:n.2000-14687_2000-14686del
NM_205863.3:c.2186-14687_2186-14686del	NP_995585.2:n.2186-14687_2186-14686del
XM_011510550.1:c.2186-14687_2186-14686del	XP_011508852.1:n.2186-14687_2186-14686del
XM_011510551.1:c.2186-14687_2186-14686del	XP_011508853.1:n.2186-14687_2186-14686del
XM_011510552.1:c.2210-14687_2210-14686del	XP_011508854.1:n.2210-14687_2210-14686del
XM_011510553.1:c.2210-14687_2210-14686del	XP_011508855.1:n.2210-14687_2210-14686del
XM_011510552.2:c.2210-14687_2210-14686del	XP_011508854.1:n.2210-14687_2210-14686del
XM_011510553.2:c.2210-14687_2210-14686del	XP_011508855.1:n.2210-14687_2210-14686del
XM_017003283.1:c.2150-14687_2150-14686del	XP_016858772.1:n.2150-14687_2150-14686del
XM_017003284.1:c.2120-14687_2120-14686del	XP_016858773.1:n.2120-14687_2120-14686del
XM_017003285.1:c.2024-14687_2024-14686del	XP_016858774.1:n.2024-14687_2024-14686del
XM_017003286.1:c.2018-14687_2018-14686del	XP_016858775.1:n.2018-14687_2018-14686del
XM_017003287.1:c.2210-14687_2210-14686del	XP_016858776.1:n.2210-14687_2210-14686del
XM_017003288.1:c.2210-14687_2210-14686del	XP_016858777.1:n.2210-14687_2210-14686del
XM_017003289.1:c.1685-14687_1685-14686del	XP_016858778.1:n.1685-14687_1685-14686del
XM_017003290.1:c.1589-14687_1589-14686del	XP_016858779.1:n.1589-14687_1589-14686del
XM_017003291.1:c.1589-14687_1589-14686del	XP_016858780.1:n.1589-14687_1589-14686del
XM_017003292.1:c.1589-14687_1589-14686del	XP_016858781.1:n.1589-14687_1589-14686del
XM_017003293.1:c.1589-14687_1589-14686del	XP_016858782.1:n.1589-14687_1589-14686del
NM_001302769.2:c.2186-14687_2186-14686del MANE Select	NP_001289698.1:n.2186-14687_2186-14686del
NM_057177.7:c.2186-15621_2186-15620del	NP_476518.4:n.2186-15621_2186-15620del
NM_152526.6:c.2000-14687_2000-14686del	NP_689739.4:n.2000-14687_2000-14686del
NM_205863.4:c.2186-14687_2186-14686del	NP_995585.2:n.2186-14687_2186-14686del