Canonical Allele Identifier: CA2068595

Gene: PARD3B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.205615652G>C , CM000664.2:g.205615652G>C	GRCh38
NC_000002.11:g.206480376G>C , CM000664.1:g.206480376G>C	GRCh37
NC_000002.10:g.206188621G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406610.7:c.3457G>C MANE Select	ENSP00000385848.2:p.Gly1153Arg
ENST00000349953.7:c.3154G>C	ENSP00000340280.3:p.Gly1052Arg
ENST00000351153.5:c.3250G>C	ENSP00000317261.2:p.Gly1084Arg
ENST00000358768.6:c.3271G>C	ENSP00000351618.2:p.Gly1091Arg
ENST00000406610.6:c.3457G>C	ENSP00000385848.2:p.Gly1153Arg
ENST00000488622.1:n.562G>C
ENST00000613457.4:c.3049G>C	ENSP00000484434.1:p.Gly1017Arg
ENST00000614500.3:c.3028G>C	ENSP00000481918.1:p.Gly1010Arg
ENST00000622699.2:c.2932G>C	ENSP00000482649.1:p.Gly978Arg
NM_001302769.1:c.3457G>C	NP_001289698.1:p.Gly1153Arg
NM_057177.6:c.3250G>C	NP_476518.4:p.Gly1084Arg
NM_152526.5:c.3271G>C	NP_689739.4:p.Gly1091Arg
NM_205863.3:c.3154G>C	NP_995585.2:p.Gly1052Arg
XM_011510550.1:c.3602G>C	XP_011508852.1:p.Arg1201Thr
XM_011510551.1:c.3542G>C	XP_011508853.1:p.Arg1181Thr
XM_011510552.1:c.3481G>C	XP_011508854.1:p.Gly1161Arg
XM_011510552.2:c.3481G>C	XP_011508854.1:p.Gly1161Arg
XM_017003283.1:c.3421G>C	XP_016858772.1:p.Gly1141Arg
XM_017003284.1:c.3391G>C	XP_016858773.1:p.Gly1131Arg
XM_017003285.1:c.3295G>C	XP_016858774.1:p.Gly1099Arg
XM_017003286.1:c.3289G>C	XP_016858775.1:p.Gly1097Arg
XM_017003288.1:c.3178G>C	XP_016858777.1:p.Gly1060Arg
XM_017003289.1:c.2956G>C	XP_016858778.1:p.Gly986Arg
XM_017003290.1:c.2860G>C	XP_016858779.1:p.Gly954Arg
XM_017003291.1:c.2860G>C	XP_016858780.1:p.Gly954Arg
XM_017003292.1:c.2860G>C	XP_016858781.1:p.Gly954Arg
XM_017003293.1:c.2860G>C	XP_016858782.1:p.Gly954Arg
NM_001302769.2:c.3457G>C MANE Select	NP_001289698.1:p.Gly1153Arg
NM_057177.7:c.3250G>C	NP_476518.4:p.Gly1084Arg
NM_152526.6:c.3271G>C	NP_689739.4:p.Gly1091Arg
NM_205863.4:c.3154G>C	NP_995585.2:p.Gly1052Arg