Canonical Allele Identifier: CA2195408558

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022584G= , CM000677.2:g.91022584G=	GRCh38
NC_000015.9:g.91565814G= , CM000677.1:g.91565814G=	GRCh37
NC_000015.8:g.89366818G=	NCBI36
NG_012162.1:g.5020C= , LRG_884:g.5020C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-335C= MANE Select	ENSP00000327650.4:n.-335C=
ENST00000333371.7:c.-335C=	ENSP00000327650.3:n.-335C=
ENST00000535906.1:c.-335C=	ENSP00000444053.1:n.-335C=
ENST00000556096.6:n.20C=
ENST00000557358.1:n.13C=
NM_001289148.1:c.-335C=	NP_001276077.1:n.-335C=
NM_001289149.1:c.-546C=	NP_001276078.1:n.-546C=
NM_018668.4:c.-335C= , LRG_884t1:c.-335C=	NP_061138.3:n.-335C=
XM_005254884.2:c.-335C=	XP_005254941.1:n.-335C=
XM_005254887.1:c.-465C=	XP_005254944.1:n.-465C=
XM_005254888.2:c.-335C=	XP_005254945.1:n.-335C=
XM_011521448.1:c.-648C=	XP_011519750.1:n.-648C=
XM_017022075.2:c.-696C=	XP_016877564.1:n.-696C=
XM_017022076.1:c.-553C=	XP_016877565.1:n.-553C=
XR_001751213.2:n.2C=
NM_018668.5:c.-335C= MANE Select	NP_061138.3:n.-335C=