Canonical Allele Identifier: CA492204121

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91545284A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91002054A>C , CM000677.2:g.91002054A>C	GRCh38
NC_000015.9:g.91545284A>C , CM000677.1:g.91545284A>C	GRCh37
NC_000015.8:g.89346288A>C	NCBI36
NG_012162.1:g.25550T>G , LRG_884:g.25550T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.1401T>G MANE Select	ENSP00000327650.4:p.Ala467=
ENST00000643536.1:c.1401T>G	ENSP00000494429.1:p.Ala467=
ENST00000647331.1:c.1401T>G	ENSP00000493953.1:p.Ala467=
ENST00000333371.7:c.1401T>G	ENSP00000327650.3:p.Ala467=
ENST00000535906.1:c.1320T>G	ENSP00000444053.1:p.Ala440=
ENST00000574755.5:c.*1096T>G	ENSP00000460413.1:n.*1096T>G
NM_001289148.1:c.1320T>G	NP_001276077.1:p.Ala440=
NM_001289149.1:c.1128T>G	NP_001276078.1:p.Ala376=
NM_018668.4:c.1401T>G , LRG_884t1:c.1401T>G	NP_061138.3:p.Ala467=
XM_005254884.2:c.1323T>G	XP_005254941.1:p.Ala441=
XM_005254887.1:c.1128T>G	XP_005254944.1:p.Ala376=
XM_011521448.1:c.1128T>G	XP_011519750.1:p.Ala376=
XM_011521449.1:c.1077T>G	XP_011519751.1:p.Ala359=
XM_011521449.2:c.1077T>G	XP_011519751.1:p.Ala359=
XM_017022075.2:c.1056T>G	XP_016877564.1:p.Ala352=
XM_017022076.1:c.1056T>G	XP_016877565.1:p.Ala352=
XR_001751213.2:n.1899T>G
NM_018668.5:c.1401T>G MANE Select	NP_061138.3:p.Ala467=