Canonical Allele Identifier: CA342250466
Gene: VPS45 HGNC NCBI

Linked Data

dbSNP Id: rs1553799314

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150081376G>A , CM000663.2:g.150081376G>A GRCh38
NC_000001.10:g.150053458G>A , CM000663.1:g.150053458G>A GRCh37
NC_000001.9:g.148320082G>A NCBI36
NG_033910.1:g.19084G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000419023.4:c.650G>A ENSP00000400143.3:p.Gly217Asp
ENST00000460366.6:n.854G>A
ENST00000477558.3:n.1227G>A
ENST00000497638.3:n.1505G>A
ENST00000642919.2:c.*619G>A ENSP00000494763.1:n.*619G>A
ENST00000643970.2:c.614G>A ENSP00000495148.1:p.Gly205Asp
ENST00000644526.2:c.722G>A ENSP00000494363.1:p.Gly241Asp
ENST00000644704.2:c.722G>A ENSP00000495981.2:p.Gly241Asp
ENST00000698523.1:c.614G>A ENSP00000513772.1:p.Gly205Asp
ENST00000698527.1:c.722G>A ENSP00000513776.1:p.Gly241Asp
ENST00000698528.1:c.722G>A ENSP00000513777.1:p.Gly241Asp
ENST00000698529.1:n.844G>A
ENST00000698530.1:n.844G>A
ENST00000698531.1:n.844G>A
ENST00000698532.1:c.653G>A ENSP00000513778.1:p.Gly218Asp
ENST00000698533.1:c.587G>A ENSP00000513779.1:p.Gly196Asp
ENST00000698534.1:c.722G>A ENSP00000513780.1:p.Gly241Asp
ENST00000698578.1:c.722G>A ENSP00000513807.1:p.Gly241Asp
ENST00000698579.1:c.722G>A ENSP00000513808.1:p.Gly241Asp
ENST00000698580.1:c.722G>A ENSP00000513809.1:p.Gly241Asp
ENST00000698581.1:c.722G>A ENSP00000513810.1:p.Gly241Asp
ENST00000698582.1:c.722G>A ENSP00000513811.1:p.Gly241Asp
ENST00000698583.1:c.722G>A ENSP00000513812.1:p.Gly241Asp
ENST00000698584.1:c.722G>A ENSP00000513813.1:p.Gly241Asp
ENST00000698585.1:c.722G>A ENSP00000513814.1:p.Gly241Asp
ENST00000698586.1:c.722G>A ENSP00000513815.1:p.Gly241Asp
ENST00000698587.1:c.758G>A ENSP00000513816.1:p.Gly253Asp
ENST00000698588.1:c.611G>A ENSP00000513817.1:p.Gly204Asp
ENST00000698589.1:n.2657G>A
ENST00000698590.1:c.719G>A ENSP00000513818.1:p.Gly240Asp
ENST00000698591.1:c.688-31G>A ENSP00000513819.1:n.688-31G>A
ENST00000698592.1:c.688-508G>A ENSP00000513820.1:n.688-508G>A
ENST00000698593.1:c.722G>A ENSP00000513821.1:p.Gly241Asp
ENST00000698594.1:c.515G>A ENSP00000513822.1:p.Gly172Asp
ENST00000698595.1:c.722G>A ENSP00000513823.1:p.Gly241Asp
ENST00000698596.1:n.1942G>A
ENST00000698597.1:c.626G>A ENSP00000513824.1:p.Gly209Asp
ENST00000698598.1:c.758G>A ENSP00000513825.1:p.Gly253Asp
ENST00000419023.3:c.650G>A ENSP00000400143.2:p.Gly217Asp
ENST00000477558.2:n.626G>A
ENST00000491789.2:c.515G>A ENSP00000494741.1:p.Gly172Asp
ENST00000642919.1:c.*619G>A ENSP00000494763.1:n.*619G>A
ENST00000643970.1:c.614G>A ENSP00000495148.1:p.Gly205Asp
ENST00000644510.2:c.722G>A MANE Select ENSP00000495563.1:p.Gly241Asp
ENST00000644526.1:c.722G>A ENSP00000494363.1:p.Gly241Asp
ENST00000644704.1:c.80G>A ENSP00000495981.1:p.Gly27Asp
ENST00000369128.9:c.407G>A ENSP00000358124.5:p.Gly136Asp
ENST00000369130.7:c.722G>A ENSP00000358126.3:p.Gly241Asp
ENST00000419023.2:c.515G>A ENSP00000400143.1:p.Gly172Asp
ENST00000462852.5:c.580-31G>A ENSP00000481356.1:n.580-31G>A
ENST00000477558.1:n.624G>A
ENST00000535106.5:c.407G>A ENSP00000440690.2:p.Gly136Asp
ENST00000611412.4:c.353G>A ENSP00000478403.1:p.Gly118Asp
NM_001279353.1:c.407G>A NP_001266282.1:p.Gly136Asp
NM_001279354.1:c.614G>A NP_001266283.1:p.Gly205Asp
NM_001279355.1:c.353G>A NP_001266284.1:p.Gly118Asp
NM_007259.4:c.722G>A NP_009190.2:p.Gly241Asp
NR_103998.1:n.705G>A
XR_921733.1:n.837G>A
XR_921734.1:n.837G>A
XR_921735.1:n.837G>A
NM_007259.5:c.722G>A MANE Select NP_009190.2:p.Gly241Asp
XM_024452791.1:c.614G>A XP_024308559.1:p.Gly205Asp
XR_921733.3:n.808G>A
XR_921734.3:n.808G>A
NM_001279353.2:c.407G>A NP_001266282.1:p.Gly136Asp
NM_001279354.2:c.614G>A NP_001266283.1:p.Gly205Asp
NR_103998.2:n.597G>A