Canonical Allele Identifier: CA393886413

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91545285G>T (hg19) ; chr15:g.91002055G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002055G>T , CM000677.2:g.91002055G>T	GRCh38
NC_000015.9:g.91545285G>T , CM000677.1:g.91545285G>T	GRCh37
NC_000015.8:g.89346289G>T	NCBI36
NG_012162.1:g.25549C>A , LRG_884:g.25549C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1400C>A MANE Select	ENSP00000327650.4:p.Ala467Asp
ENST00000643536.1:c.1400C>A	ENSP00000494429.1:p.Ala467Asp
ENST00000647331.1:c.1400C>A	ENSP00000493953.1:p.Ala467Asp
ENST00000333371.7:c.1400C>A	ENSP00000327650.3:p.Ala467Asp
ENST00000535906.1:c.1319C>A	ENSP00000444053.1:p.Ala440Asp
ENST00000574755.5:c.*1095C>A	ENSP00000460413.1:n.*1095C>A
NM_001289148.1:c.1319C>A	NP_001276077.1:p.Ala440Asp
NM_001289149.1:c.1127C>A	NP_001276078.1:p.Ala376Asp
NM_018668.4:c.1400C>A , LRG_884t1:c.1400C>A	NP_061138.3:p.Ala467Asp
XM_005254884.2:c.1322C>A	XP_005254941.1:p.Ala441Asp
XM_005254887.1:c.1127C>A	XP_005254944.1:p.Ala376Asp
XM_011521448.1:c.1127C>A	XP_011519750.1:p.Ala376Asp
XM_011521449.1:c.1076C>A	XP_011519751.1:p.Ala359Asp
XM_011521449.2:c.1076C>A	XP_011519751.1:p.Ala359Asp
XM_017022075.2:c.1055C>A	XP_016877564.1:p.Ala352Asp
XM_017022076.1:c.1055C>A	XP_016877565.1:p.Ala352Asp
XR_001751213.2:n.1898C>A
NM_018668.5:c.1400C>A MANE Select	NP_061138.3:p.Ala467Asp