Canonical Allele Identifier: CA3817646

Gene: CUL9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43196791C>T , CM000668.2:g.43196791C>T	GRCh38
NC_000006.11:g.43164529C>T , CM000668.1:g.43164529C>T	GRCh37
NC_000006.10:g.43272507C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015089.4:c.2732C>T MANE Select	NP_055904.1:p.Pro911Leu
ENST00000252050.9:c.2732C>T MANE Select	ENSP00000252050.4:p.Pro911Leu
NM_015089.3:c.2732C>T	NP_055904.1:p.Pro911Leu
ENST00000252050.8:c.2732C>T	ENSP00000252050.4:p.Pro911Leu
ENST00000372647.6:c.2732C>T	ENSP00000361730.2:p.Pro911Leu
ENST00000515773.5:n.3186C>T
XM_011514422.1:c.2732C>T	XP_011512724.1:p.Pro911Leu
XM_011514423.1:c.2732C>T	XP_011512725.1:p.Pro911Leu
XM_011514423.2:c.2732C>T	XP_011512725.1:p.Pro911Leu
XM_011514424.1:c.2732C>T	XP_011512726.1:p.Pro911Leu
XM_011514425.1:c.2402C>T	XP_011512727.1:p.Pro801Leu
XM_011514426.1:c.2732C>T	XP_011512728.1:p.Pro911Leu
XM_011514427.1:c.1319C>T	XP_011512729.1:p.Pro440Leu
XM_011514428.1:c.2732C>T	XP_011512730.1:p.Pro911Leu
XM_011514429.1:c.536C>T	XP_011512731.1:p.Pro179Leu
XM_011514430.1:c.2732C>T	XP_011512732.1:p.Pro911Leu
XM_017010589.1:c.2732C>T	XP_016866078.1:p.Pro911Leu
XM_017010590.1:c.761C>T	XP_016866079.1:p.Pro254Leu
XR_001743278.2:n.2816C>T
XR_001743281.1:n.2816C>T
XR_002956271.1:n.2816C>T
XR_926122.1:n.2816C>T
XR_926123.1:n.2816C>T