Canonical Allele Identifier: CA2630423975

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022444-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022444_91022445insT , CM000677.2:g.91022444_91022445insT	GRCh38
NC_000015.9:g.91565674_91565675insT , CM000677.1:g.91565674_91565675insT	GRCh37
NC_000015.8:g.89366678_89366679insT	NCBI36
NG_012162.1:g.5159_5160insA , LRG_884:g.5159_5160insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-196_-195insA MANE Select	ENSP00000327650.4:n.-196_-195insA
ENST00000643536.1:c.-196_-195insA	ENSP00000494429.1:n.-196_-195insA
ENST00000333371.7:c.-196_-195insA	ENSP00000327650.3:n.-196_-195insA
ENST00000535906.1:c.-196_-195insA	ENSP00000444053.1:n.-196_-195insA
ENST00000556096.6:n.159_160insA
ENST00000557358.1:n.152_153insA
ENST00000574755.5:c.-196_-195insA	ENSP00000460413.1:n.-196_-195insA
NM_001289148.1:c.-196_-195insA	NP_001276077.1:n.-196_-195insA
NM_001289149.1:c.-407_-406insA	NP_001276078.1:n.-407_-406insA
NM_018668.4:c.-196_-195insA , LRG_884t1:c.-196_-195insA	NP_061138.3:n.-196_-195insA
XM_005254884.2:c.-196_-195insA	XP_005254941.1:n.-196_-195insA
XM_005254887.1:c.-326_-325insA	XP_005254944.1:n.-326_-325insA
XM_005254888.2:c.-196_-195insA	XP_005254945.1:n.-196_-195insA
XM_011521448.1:c.-509_-508insA	XP_011519750.1:n.-509_-508insA
XM_017022075.2:c.-557_-556insA	XP_016877564.1:n.-557_-556insA
XM_017022076.1:c.-414_-413insA	XP_016877565.1:n.-414_-413insA
XR_001751213.2:n.141_142insA
NM_018668.5:c.-196_-195insA MANE Select	NP_061138.3:n.-196_-195insA