Canonical Allele Identifier: CA2195408449

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022396C= , CM000677.2:g.91022396C=	GRCh38
NC_000015.9:g.91565626C= , CM000677.1:g.91565626C=	GRCh37
NC_000015.8:g.89366630C=	NCBI36
NG_012162.1:g.5208G= , LRG_884:g.5208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-147G= MANE Select	ENSP00000327650.4:n.-147G=
ENST00000643536.1:c.-147G=	ENSP00000494429.1:n.-147G=
ENST00000333371.7:c.-147G=	ENSP00000327650.3:n.-147G=
ENST00000535906.1:c.-147G=	ENSP00000444053.1:n.-147G=
ENST00000556096.6:n.208G=
ENST00000557358.1:n.201G=
ENST00000574755.5:c.-147G=	ENSP00000460413.1:n.-147G=
NM_001289148.1:c.-147G=	NP_001276077.1:n.-147G=
NM_001289149.1:c.-358G=	NP_001276078.1:n.-358G=
NM_018668.4:c.-147G= , LRG_884t1:c.-147G=	NP_061138.3:n.-147G=
XM_005254884.2:c.-147G=	XP_005254941.1:n.-147G=
XM_005254887.1:c.-277G=	XP_005254944.1:n.-277G=
XM_005254888.2:c.-147G=	XP_005254945.1:n.-147G=
XM_011521448.1:c.-460G=	XP_011519750.1:n.-460G=
XM_017022075.2:c.-508G=	XP_016877564.1:n.-508G=
XM_017022076.1:c.-365G=	XP_016877565.1:n.-365G=
XR_001751213.2:n.190G=
NM_018668.5:c.-147G= MANE Select	NP_061138.3:n.-147G=