Canonical Allele Identifier: CA342250692

Gene: VPS45

Linked Data

• MyVariant Identifiers: chr1:g.150053548T>G (hg19) ; chr1:g.150081466T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150081466T>G , CM000663.2:g.150081466T>G	GRCh38
NC_000001.10:g.150053548T>G , CM000663.1:g.150053548T>G	GRCh37
NC_000001.9:g.148320172T>G	NCBI36
NG_033910.1:g.19174T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419023.4:c.740T>G	ENSP00000400143.3:p.Phe247Cys
ENST00000460366.6:n.944T>G
ENST00000477558.3:n.1317T>G
ENST00000497638.3:n.1595T>G
ENST00000642919.2:c.*709T>G	ENSP00000494763.1:n.*709T>G
ENST00000643970.2:c.704T>G	ENSP00000495148.1:p.Phe235Cys
ENST00000644526.2:c.812T>G	ENSP00000494363.1:p.Phe271Cys
ENST00000644704.2:c.812T>G	ENSP00000495981.2:p.Phe271Cys
ENST00000698523.1:c.704T>G	ENSP00000513772.1:p.Phe235Cys
ENST00000698527.1:c.812T>G	ENSP00000513776.1:p.Phe271Cys
ENST00000698528.1:c.812T>G	ENSP00000513777.1:p.Phe271Cys
ENST00000698529.1:n.934T>G
ENST00000698530.1:n.934T>G
ENST00000698531.1:n.934T>G
ENST00000698532.1:c.743T>G	ENSP00000513778.1:p.Phe248Cys
ENST00000698533.1:c.677T>G	ENSP00000513779.1:p.Phe226Cys
ENST00000698534.1:c.812T>G	ENSP00000513780.1:p.Phe271Cys
ENST00000698578.1:c.812T>G	ENSP00000513807.1:p.Phe271Cys
ENST00000698579.1:c.812T>G	ENSP00000513808.1:p.Phe271Cys
ENST00000698580.1:c.812T>G	ENSP00000513809.1:p.Phe271Cys
ENST00000698581.1:c.812T>G	ENSP00000513810.1:p.Phe271Cys
ENST00000698582.1:c.812T>G	ENSP00000513811.1:p.Phe271Cys
ENST00000698583.1:c.812T>G	ENSP00000513812.1:p.Phe271Cys
ENST00000698584.1:c.812T>G	ENSP00000513813.1:p.Phe271Cys
ENST00000698585.1:c.812T>G	ENSP00000513814.1:p.Phe271Cys
ENST00000698586.1:c.812T>G	ENSP00000513815.1:p.Phe271Cys
ENST00000698587.1:c.848T>G	ENSP00000513816.1:p.Phe283Cys
ENST00000698588.1:c.701T>G	ENSP00000513817.1:p.Phe234Cys
ENST00000698589.1:n.2747T>G
ENST00000698590.1:c.809T>G	ENSP00000513818.1:p.Phe270Cys
ENST00000698591.1:c.*42T>G	ENSP00000513819.1:n.*42T>G
ENST00000698592.1:c.688-418T>G	ENSP00000513820.1:n.688-418T>G
ENST00000698593.1:c.812T>G	ENSP00000513821.1:p.Phe271Cys
ENST00000698594.1:c.605T>G	ENSP00000513822.1:p.Phe202Cys
ENST00000698595.1:c.812T>G	ENSP00000513823.1:p.Phe271Cys
ENST00000698596.1:n.2032T>G
ENST00000698597.1:c.716T>G	ENSP00000513824.1:p.Phe239Cys
ENST00000698598.1:c.848T>G	ENSP00000513825.1:p.Phe283Cys
ENST00000419023.3:c.740T>G	ENSP00000400143.2:p.Phe247Cys
ENST00000477558.2:n.716T>G
ENST00000491789.2:c.605T>G	ENSP00000494741.1:p.Phe202Cys
ENST00000642919.1:c.*709T>G	ENSP00000494763.1:n.*709T>G
ENST00000643970.1:c.704T>G	ENSP00000495148.1:p.Phe235Cys
ENST00000644510.2:c.812T>G MANE Select	ENSP00000495563.1:p.Phe271Cys
ENST00000644526.1:c.812T>G	ENSP00000494363.1:p.Phe271Cys
ENST00000644704.1:c.170T>G	ENSP00000495981.1:p.Phe57Cys
ENST00000369128.9:c.497T>G	ENSP00000358124.5:p.Phe166Cys
ENST00000369130.7:c.812T>G	ENSP00000358126.3:p.Phe271Cys
ENST00000419023.2:c.605T>G	ENSP00000400143.1:p.Phe202Cys
ENST00000462852.5:c.*42T>G	ENSP00000481356.1:n.*42T>G
ENST00000477558.1:n.714T>G
ENST00000535106.5:c.497T>G	ENSP00000440690.2:p.Phe166Cys
ENST00000611412.4:c.443T>G	ENSP00000478403.1:p.Phe148Cys
NM_001279353.1:c.497T>G	NP_001266282.1:p.Phe166Cys
NM_001279354.1:c.704T>G	NP_001266283.1:p.Phe235Cys
NM_001279355.1:c.443T>G	NP_001266284.1:p.Phe148Cys
NM_007259.4:c.812T>G	NP_009190.2:p.Phe271Cys
NR_103998.1:n.795T>G
XR_921733.1:n.927T>G
XR_921734.1:n.927T>G
XR_921735.1:n.927T>G
NM_007259.5:c.812T>G MANE Select	NP_009190.2:p.Phe271Cys
XM_024452791.1:c.704T>G	XP_024308559.1:p.Phe235Cys
XR_921733.3:n.898T>G
XR_921734.3:n.898T>G
NM_001279353.2:c.497T>G	NP_001266282.1:p.Phe166Cys
NM_001279354.2:c.704T>G	NP_001266283.1:p.Phe235Cys
NR_103998.2:n.687T>G