Canonical Allele Identifier: CA7744874

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91006024A>G , CM000677.2:g.91006024A>G	GRCh38
NC_000015.9:g.91549254A>G , CM000677.1:g.91549254A>G	GRCh37
NC_000015.8:g.89350258A>G	NCBI36
NG_012162.1:g.21580T>C , LRG_884:g.21580T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018668.5:c.888T>C MANE Select	NP_061138.3:p.Asn296=
ENST00000333371.8:c.888T>C MANE Select	ENSP00000327650.4:p.Asn296=
NM_001289148.1:c.807T>C	NP_001276077.1:p.Asn269=
NM_001289149.1:c.615T>C	NP_001276078.1:p.Asn205=
NM_018668.4:c.888T>C , LRG_884t1:c.888T>C	NP_061138.3:p.Asn296=
ENST00000333371.7:c.888T>C	ENSP00000327650.3:p.Asn296=
ENST00000535906.1:c.807T>C	ENSP00000444053.1:p.Asn269=
ENST00000556096.6:n.1708T>C
ENST00000574755.5:c.*583T>C	ENSP00000460413.1:n.*583T>C
ENST00000643536.1:c.888T>C	ENSP00000494429.1:p.Asn296=
ENST00000647331.1:c.888T>C	ENSP00000493953.1:p.Asn296=
XM_005254884.2:c.810T>C	XP_005254941.1:p.Asn270=
XM_005254887.1:c.615T>C	XP_005254944.1:p.Asn205=
XM_005254888.2:c.888T>C	XP_005254945.1:p.Asn296=
XM_011521448.1:c.615T>C	XP_011519750.1:p.Asn205=
XM_011521449.1:c.564T>C	XP_011519751.1:p.Asn188=
XM_011521449.2:c.564T>C	XP_011519751.1:p.Asn188=
XM_017022075.2:c.543T>C	XP_016877564.1:p.Asn181=
XM_017022076.1:c.543T>C	XP_016877565.1:p.Asn181=
XR_001751213.2:n.1224T>C