Canonical Allele Identifier: CA2195408376

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022247C= , CM000677.2:g.91022247C=	GRCh38
NC_000015.9:g.91565477C= , CM000677.1:g.91565477C=	GRCh37
NC_000015.8:g.89366481C=	NCBI36
NG_012162.1:g.5357G= , LRG_884:g.5357G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.3G= MANE Select	ENSP00000327650.4:p.Met1=
ENST00000643536.1:c.3G=	ENSP00000494429.1:p.Met1=
ENST00000647331.1:c.3G=	ENSP00000493953.1:p.Met1=
ENST00000333371.7:c.3G=	ENSP00000327650.3:p.Met1=
ENST00000535906.1:c.3G=	ENSP00000444053.1:p.Met1=
ENST00000556096.6:n.357G=
ENST00000557358.1:n.350G=
ENST00000574755.5:c.3G=	ENSP00000460413.1:p.Met1=
NM_001289148.1:c.3G=	NP_001276077.1:p.Met1=
NM_001289149.1:c.-209G=	NP_001276078.1:n.-209G=
NM_018668.4:c.3G= , LRG_884t1:c.3G=	NP_061138.3:p.Met1=
XM_005254884.2:c.3G=	XP_005254941.1:p.Met1=
XM_005254887.1:c.-128G=	XP_005254944.1:n.-128G=
XM_005254888.2:c.3G=	XP_005254945.1:p.Met1=
XM_011521448.1:c.-311G=	XP_011519750.1:n.-311G=
XM_017022075.2:c.-359G=	XP_016877564.1:n.-359G=
XM_017022076.1:c.-216G=	XP_016877565.1:n.-216G=
XR_001751213.2:n.339G=
NM_018668.5:c.3G= MANE Select	NP_061138.3:p.Met1=