Canonical Allele Identifier: CA425394406

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535373G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312506G>T , CM000664.2:g.27312506G>T	GRCh38
NC_000002.11:g.27535373G>T , CM000664.1:g.27535373G>T	GRCh37
NC_000002.10:g.27388877G>T	NCBI36
NG_008075.1:g.15059C>A
NG_033055.1:g.758C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.363C>A MANE Select	ENSP00000369383.1:p.Ala121=
ENST00000233545.6:c.363C>A	ENSP00000233545.2:p.Ala121=
ENST00000357186.10:c.195C>A	ENSP00000349713.6:p.Ala65=
ENST00000380044.5:c.363C>A	ENSP00000369383.1:p.Ala121=
ENST00000402310.5:c.363C>A	ENSP00000383955.1:p.Ala121=
ENST00000402722.5:c.*28C>A	ENSP00000386000.1:n.*28C>A
ENST00000403262.6:c.363C>A	ENSP00000385671.1:p.Ala121=
ENST00000405076.5:c.187-260C>A	ENSP00000385175.1:n.187-260C>A
ENST00000405983.5:c.408C>A	ENSP00000384586.1:p.Ala136=
ENST00000415514.5:c.*164C>A	ENSP00000388043.1:n.*164C>A
ENST00000426513.6:c.*28C>A	ENSP00000403824.2:n.*28C>A
ENST00000428910.5:c.285C>A	ENSP00000405235.1:p.Ala95=
ENST00000430991.5:c.209+174C>A
ENST00000475085.1:n.391C>A
ENST00000616446.1:n.340C>A
ENST00000616707.1:n.882C>A
ENST00000617583.4:n.389C>A
ENST00000621183.4:n.419C>A
ENST00000621470.4:n.379C>A
ENST00000622003.4:n.536C>A
NM_002437.4:c.363C>A	NP_002428.1:p.Ala121=
XM_005264326.2:c.363C>A	XP_005264383.1:p.Ala121=
XM_005264327.2:c.204C>A	XP_005264384.1:p.Ala68=
XM_006712021.2:c.315C>A	XP_006712084.1:p.Ala105=
XM_005264326.4:c.363C>A	XP_005264383.1:p.Ala121=
XM_006712021.3:c.315C>A	XP_006712084.1:p.Ala105=
XM_017004150.1:c.345C>A	XP_016859639.1:p.Ala115=
XM_017004151.1:c.315C>A	XP_016859640.1:p.Ala105=
XM_017004152.1:c.204C>A	XP_016859641.1:p.Ala68=
XM_024452913.1:c.315C>A	XP_024308681.1:p.Ala105=
NM_002437.5:c.363C>A MANE Select	NP_002428.1:p.Ala121=