Canonical Allele Identifier: CA492173219

Gene: VPS33B

Linked Data

• MyVariant Identifiers: chr15:g.91557662A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91014432A>G , CM000677.2:g.91014432A>G	GRCh38
NC_000015.9:g.91557662A>G , CM000677.1:g.91557662A>G	GRCh37
NC_000015.8:g.89358666A>G	NCBI36
NG_012162.1:g.13172T>C , LRG_884:g.13172T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333371.8:c.241T>C MANE Select	ENSP00000327650.4:p.Leu81=
ENST00000643536.1:c.241T>C	ENSP00000494429.1:p.Leu81=
ENST00000647331.1:c.241T>C	ENSP00000493953.1:p.Leu81=
ENST00000333371.7:c.241T>C	ENSP00000327650.3:p.Leu81=
ENST00000535906.1:c.160T>C	ENSP00000444053.1:p.Leu54=
ENST00000554264.5:n.164T>C
ENST00000556096.6:n.635T>C
ENST00000557358.1:n.445T>C
ENST00000574755.5:c.179T>C	ENSP00000460413.1:p.Ile60Thr
NM_001289148.1:c.160T>C	NP_001276077.1:p.Leu54=
NM_001289149.1:c.-33T>C	NP_001276078.1:n.-33T>C
NM_018668.4:c.241T>C , LRG_884t1:c.241T>C	NP_061138.3:p.Leu81=
XM_005254884.2:c.241T>C	XP_005254941.1:p.Leu81=
XM_005254887.1:c.-33T>C	XP_005254944.1:n.-33T>C
XM_005254888.2:c.241T>C	XP_005254945.1:p.Leu81=
XM_011521448.1:c.-33T>C	XP_011519750.1:n.-33T>C
XM_017022075.2:c.-121T>C	XP_016877564.1:n.-121T>C
XM_017022076.1:c.-121T>C	XP_016877565.1:n.-121T>C
XR_001751213.2:n.577T>C
NM_018668.5:c.241T>C MANE Select	NP_061138.3:p.Leu81=