Canonical Allele Identifier: CA2195408402

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022294_91022295delinsCT , CM000677.2:g.91022294_91022295delinsCT	GRCh38
NC_000015.9:g.91565524_91565525delinsCT , CM000677.1:g.91565524_91565525delinsCT	GRCh37
NC_000015.8:g.89366528_89366529delinsCT	NCBI36
NG_012162.1:g.5309_5310delinsAG , LRG_884:g.5309_5310delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-46_-45delinsAG MANE Select	ENSP00000327650.4:n.-46_-45delinsAG
ENST00000643536.1:c.-46_-45delinsAG	ENSP00000494429.1:n.-46_-45delinsAG
ENST00000333371.7:c.-46_-45delinsAG	ENSP00000327650.3:n.-46_-45delinsAG
ENST00000535906.1:c.-46_-45delinsAG	ENSP00000444053.1:n.-46_-45delinsAG
ENST00000556096.6:n.309_310delinsAG
ENST00000557358.1:n.302_303delinsAG
ENST00000574755.5:c.-46_-45delinsAG	ENSP00000460413.1:n.-46_-45delinsAG
NM_001289148.1:c.-46_-45delinsAG	NP_001276077.1:n.-46_-45delinsAG
NM_001289149.1:c.-257_-256delinsAG	NP_001276078.1:n.-257_-256delinsAG
NM_018668.4:c.-46_-45delinsAG , LRG_884t1:c.-46_-45delinsAG	NP_061138.3:n.-46_-45delinsAG
XM_005254884.2:c.-46_-45delinsAG	XP_005254941.1:n.-46_-45delinsAG
XM_005254887.1:c.-176_-175delinsAG	XP_005254944.1:n.-176_-175delinsAG
XM_005254888.2:c.-46_-45delinsAG	XP_005254945.1:n.-46_-45delinsAG
XM_011521448.1:c.-359_-358delinsAG	XP_011519750.1:n.-359_-358delinsAG
XM_017022075.2:c.-407_-406delinsAG	XP_016877564.1:n.-407_-406delinsAG
XM_017022076.1:c.-264_-263delinsAG	XP_016877565.1:n.-264_-263delinsAG
XR_001751213.2:n.291_292delinsAG
NM_018668.5:c.-46_-45delinsAG MANE Select	NP_061138.3:n.-46_-45delinsAG