Canonical Allele Identifier: CA2581236130

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91001981C>A , CM000677.2:g.91001981C>A	GRCh38
NC_000015.9:g.91545211C>A , CM000677.1:g.91545211C>A	GRCh37
NC_000015.8:g.89346215C>A	NCBI36
NG_012162.1:g.25623G>T , LRG_884:g.25623G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1405+69G>T MANE Select	ENSP00000327650.4:n.1405+69G>T
ENST00000643536.1:c.1405+69G>T	ENSP00000494429.1:n.1405+69G>T
ENST00000647331.1:c.1405+69G>T	ENSP00000493953.1:n.1405+69G>T
ENST00000333371.7:c.1405+69G>T	ENSP00000327650.3:n.1405+69G>T
ENST00000535906.1:c.1324+69G>T	ENSP00000444053.1:n.1324+69G>T
ENST00000574755.5:c.*1100+69G>T	ENSP00000460413.1:n.*1100+69G>T
NM_001289148.1:c.1324+69G>T	NP_001276077.1:n.1324+69G>T
NM_001289149.1:c.1132+69G>T	NP_001276078.1:n.1132+69G>T
NM_018668.4:c.1405+69G>T , LRG_884t1:c.1405+69G>T	NP_061138.3:n.1405+69G>T
XM_005254884.2:c.1327+69G>T	XP_005254941.1:n.1327+69G>T
XM_005254887.1:c.1132+69G>T	XP_005254944.1:n.1132+69G>T
XM_011521448.1:c.1132+69G>T	XP_011519750.1:n.1132+69G>T
XM_011521449.1:c.1081+69G>T	XP_011519751.1:n.1081+69G>T
XM_011521449.2:c.1081+69G>T	XP_011519751.1:n.1081+69G>T
XM_017022075.2:c.1060+69G>T	XP_016877564.1:n.1060+69G>T
XM_017022076.1:c.1060+69G>T	XP_016877565.1:n.1060+69G>T
XR_001751213.2:n.1903+69G>T
NM_018668.5:c.1405+69G>T MANE Select	NP_061138.3:n.1405+69G>T