Canonical Allele Identifier: CA393860748

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91557630A>T (hg19) ; chr15:g.91014400A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91014400A>T , CM000677.2:g.91014400A>T	GRCh38
NC_000015.9:g.91557630A>T , CM000677.1:g.91557630A>T	GRCh37
NC_000015.8:g.89358634A>T	NCBI36
NG_012162.1:g.13204T>A , LRG_884:g.13204T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.273T>A MANE Select	ENSP00000327650.4:p.Asn91Lys
ENST00000643536.1:c.273T>A	ENSP00000494429.1:p.Asn91Lys
ENST00000647331.1:c.273T>A	ENSP00000493953.1:p.Asn91Lys
ENST00000333371.7:c.273T>A	ENSP00000327650.3:p.Asn91Lys
ENST00000535906.1:c.192T>A	ENSP00000444053.1:p.Asn64Lys
ENST00000554264.5:n.196T>A
ENST00000556096.6:n.667T>A
ENST00000557358.1:n.477T>A
ENST00000574755.5:c.211T>A	ENSP00000460413.1:p.Tyr71Asn
NM_001289148.1:c.192T>A	NP_001276077.1:p.Asn64Lys
NM_001289149.1:c.-1T>A	NP_001276078.1:n.-1T>A
NM_018668.4:c.273T>A , LRG_884t1:c.273T>A	NP_061138.3:p.Asn91Lys
XM_005254884.2:c.273T>A	XP_005254941.1:p.Asn91Lys
XM_005254887.1:c.-1T>A	XP_005254944.1:n.-1T>A
XM_005254888.2:c.273T>A	XP_005254945.1:p.Asn91Lys
XM_011521448.1:c.-1T>A	XP_011519750.1:n.-1T>A
XM_017022075.2:c.-89T>A	XP_016877564.1:n.-89T>A
XM_017022076.1:c.-89T>A	XP_016877565.1:n.-89T>A
XR_001751213.2:n.609T>A
NM_018668.5:c.273T>A MANE Select	NP_061138.3:p.Asn91Lys