Canonical Allele Identifier: CA393860762

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91014406-G-C
• MyVariant Identifiers: chr15:g.91557636G>C (hg19) ; chr15:g.91014406G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91014406G>C , CM000677.2:g.91014406G>C	GRCh38
NC_000015.9:g.91557636G>C , CM000677.1:g.91557636G>C	GRCh37
NC_000015.8:g.89358640G>C	NCBI36
NG_012162.1:g.13198C>G , LRG_884:g.13198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.267C>G MANE Select	ENSP00000327650.4:p.Ile89Met
ENST00000643536.1:c.267C>G	ENSP00000494429.1:p.Ile89Met
ENST00000647331.1:c.267C>G	ENSP00000493953.1:p.Ile89Met
ENST00000333371.7:c.267C>G	ENSP00000327650.3:p.Ile89Met
ENST00000535906.1:c.186C>G	ENSP00000444053.1:p.Ile62Met
ENST00000554264.5:n.190C>G
ENST00000556096.6:n.661C>G
ENST00000557358.1:n.471C>G
ENST00000574755.5:c.205C>G	ENSP00000460413.1:p.Gln69Glu
NM_001289148.1:c.186C>G	NP_001276077.1:p.Ile62Met
NM_001289149.1:c.-7C>G	NP_001276078.1:n.-7C>G
NM_018668.4:c.267C>G , LRG_884t1:c.267C>G	NP_061138.3:p.Ile89Met
XM_005254884.2:c.267C>G	XP_005254941.1:p.Ile89Met
XM_005254887.1:c.-7C>G	XP_005254944.1:n.-7C>G
XM_005254888.2:c.267C>G	XP_005254945.1:p.Ile89Met
XM_011521448.1:c.-7C>G	XP_011519750.1:n.-7C>G
XM_017022075.2:c.-95C>G	XP_016877564.1:n.-95C>G
XM_017022076.1:c.-95C>G	XP_016877565.1:n.-95C>G
XR_001751213.2:n.603C>G
NM_018668.5:c.267C>G MANE Select	NP_061138.3:p.Ile89Met