Canonical Allele Identifier: CA350141157

Gene: PARD3B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.204686205C>G , CM000664.2:g.204686205C>G	GRCh38
NC_000002.11:g.205550928C>G , CM000664.1:g.205550928C>G	GRCh37
NC_000002.10:g.205259173C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001302769.2:c.145C>G MANE Select	NP_001289698.1:p.His49Asp
ENST00000406610.7:c.145C>G MANE Select	ENSP00000385848.2:p.His49Asp
NM_001302769.1:c.145C>G	NP_001289698.1:p.His49Asp
NM_057177.6:c.145C>G	NP_476518.4:p.His49Asp
NM_057177.7:c.145C>G	NP_476518.4:p.His49Asp
NM_152526.5:c.145C>G	NP_689739.4:p.His49Asp
NM_152526.6:c.145C>G	NP_689739.4:p.His49Asp
NM_205863.3:c.145C>G	NP_995585.2:p.His49Asp
NM_205863.4:c.145C>G	NP_995585.2:p.His49Asp
ENST00000349953.7:c.145C>G	ENSP00000340280.3:p.His49Asp
ENST00000351153.5:c.145C>G	ENSP00000317261.2:p.His49Asp
ENST00000358768.6:c.145C>G	ENSP00000351618.2:p.His49Asp
ENST00000406610.6:c.145C>G	ENSP00000385848.2:p.His49Asp
ENST00000415947.1:c.197C>G	ENSP00000407718.1:p.Ser66Ter
ENST00000462231.5:c.145C>G	ENSP00000473503.1:p.His49Asp
XM_011510550.1:c.145C>G	XP_011508852.1:p.His49Asp
XM_011510551.1:c.145C>G	XP_011508853.1:p.His49Asp
XM_011510552.1:c.169C>G	XP_011508854.1:p.His57Asp
XM_011510552.2:c.169C>G	XP_011508854.1:p.His57Asp
XM_011510553.1:c.169C>G	XP_011508855.1:p.His57Asp
XM_011510553.2:c.169C>G	XP_011508855.1:p.His57Asp
XM_017003285.1:c.169C>G	XP_016858774.1:p.His57Asp
XM_017003287.1:c.169C>G	XP_016858776.1:p.His57Asp
XM_017003288.1:c.169C>G	XP_016858777.1:p.His57Asp
XM_017003290.1:c.-453C>G	XP_016858779.1:n.-453C>G
XM_017003291.1:c.-453C>G	XP_016858780.1:n.-453C>G
XM_017003292.1:c.-453C>G	XP_016858781.1:n.-453C>G
XM_017003294.1:c.169C>G	XP_016858783.1:p.His57Asp