Canonical Allele Identifier: CA2195408437

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022373G= , CM000677.2:g.91022373G=	GRCh38
NC_000015.9:g.91565603G= , CM000677.1:g.91565603G=	GRCh37
NC_000015.8:g.89366607G=	NCBI36
NG_012162.1:g.5231C= , LRG_884:g.5231C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-124C= MANE Select	ENSP00000327650.4:n.-124C=
ENST00000643536.1:c.-124C=	ENSP00000494429.1:n.-124C=
ENST00000333371.7:c.-124C=	ENSP00000327650.3:n.-124C=
ENST00000535906.1:c.-124C=	ENSP00000444053.1:n.-124C=
ENST00000556096.6:n.231C=
ENST00000557358.1:n.224C=
ENST00000574755.5:c.-124C=	ENSP00000460413.1:n.-124C=
NM_001289148.1:c.-124C=	NP_001276077.1:n.-124C=
NM_001289149.1:c.-335C=	NP_001276078.1:n.-335C=
NM_018668.4:c.-124C= , LRG_884t1:c.-124C=	NP_061138.3:n.-124C=
XM_005254884.2:c.-124C=	XP_005254941.1:n.-124C=
XM_005254887.1:c.-254C=	XP_005254944.1:n.-254C=
XM_005254888.2:c.-124C=	XP_005254945.1:n.-124C=
XM_011521448.1:c.-437C=	XP_011519750.1:n.-437C=
XM_017022075.2:c.-485C=	XP_016877564.1:n.-485C=
XM_017022076.1:c.-342C=	XP_016877565.1:n.-342C=
XR_001751213.2:n.213C=
NM_018668.5:c.-124C= MANE Select	NP_061138.3:n.-124C=