Canonical Allele Identifier: CA346205401

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27532818A>C (hg19) ; chr2:g.27309950A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309950A>C , CM000664.2:g.27309950A>C	GRCh38
NC_000002.11:g.27532818A>C , CM000664.1:g.27532818A>C	GRCh37
NC_000002.10:g.27386322A>C	NCBI36
NG_008075.1:g.17614T>G
NG_033055.1:g.3313T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.493T>G MANE Select	ENSP00000369383.1:p.Trp165Gly
ENST00000233545.6:c.493T>G	ENSP00000233545.2:p.Trp165Gly
ENST00000357186.10:c.325T>G	ENSP00000349713.6:p.Trp109Gly
ENST00000380044.5:c.493T>G	ENSP00000369383.1:p.Trp165Gly
ENST00000402310.5:c.440T>G	ENSP00000383955.1:p.Leu147Arg
ENST00000402722.5:c.*72T>G	ENSP00000386000.1:n.*72T>G
ENST00000405076.5:c.304T>G	ENSP00000385175.1:p.Trp102Gly
ENST00000405983.5:c.538T>G	ENSP00000384586.1:p.Trp180Gly
ENST00000415514.5:c.*294T>G	ENSP00000388043.1:n.*294T>G
ENST00000426513.6:c.*158T>G	ENSP00000403824.2:n.*158T>G
ENST00000430991.5:c.327T>G
ENST00000620797.4:n.166T>G
ENST00000621183.4:n.796T>G
NM_002437.4:c.493T>G	NP_002428.1:p.Trp165Gly
XM_005264326.2:c.493T>G	XP_005264383.1:p.Trp165Gly
XM_005264327.2:c.334T>G	XP_005264384.1:p.Trp112Gly
XM_006712021.2:c.445T>G	XP_006712084.1:p.Trp149Gly
XM_005264326.4:c.493T>G	XP_005264383.1:p.Trp165Gly
XM_006712021.3:c.445T>G	XP_006712084.1:p.Trp149Gly
XM_017004150.1:c.475T>G	XP_016859639.1:p.Trp159Gly
XM_017004151.1:c.445T>G	XP_016859640.1:p.Trp149Gly
XM_017004152.1:c.334T>G	XP_016859641.1:p.Trp112Gly
XM_024452913.1:c.445T>G	XP_024308681.1:p.Trp149Gly
NM_002437.5:c.493T>G MANE Select	NP_002428.1:p.Trp165Gly