Canonical Allele Identifier: CA346207828

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535372T>C (hg19) ; chr2:g.27312505T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312505T>C , CM000664.2:g.27312505T>C	GRCh38
NC_000002.11:g.27535372T>C , CM000664.1:g.27535372T>C	GRCh37
NC_000002.10:g.27388876T>C	NCBI36
NG_008075.1:g.15060A>G
NG_033055.1:g.759A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.364A>G MANE Select	ENSP00000369383.1:p.Lys122Glu
ENST00000233545.6:c.364A>G	ENSP00000233545.2:p.Lys122Glu
ENST00000357186.10:c.196A>G	ENSP00000349713.6:p.Lys66Glu
ENST00000380044.5:c.364A>G	ENSP00000369383.1:p.Lys122Glu
ENST00000402310.5:c.364A>G	ENSP00000383955.1:p.Lys122Glu
ENST00000402722.5:c.*29A>G	ENSP00000386000.1:n.*29A>G
ENST00000403262.6:c.364A>G	ENSP00000385671.1:p.Lys122Glu
ENST00000405076.5:c.187-259A>G	ENSP00000385175.1:n.187-259A>G
ENST00000405983.5:c.409A>G	ENSP00000384586.1:p.Lys137Glu
ENST00000415514.5:c.*165A>G	ENSP00000388043.1:n.*165A>G
ENST00000426513.6:c.*29A>G	ENSP00000403824.2:n.*29A>G
ENST00000428910.5:c.286A>G	ENSP00000405235.1:p.Lys96Glu
ENST00000430991.5:c.209+175A>G
ENST00000475085.1:n.392A>G
ENST00000616446.1:n.341A>G
ENST00000616707.1:n.883A>G
ENST00000617583.4:n.390A>G
ENST00000621183.4:n.420A>G
ENST00000621470.4:n.380A>G
ENST00000622003.4:n.537A>G
NM_002437.4:c.364A>G	NP_002428.1:p.Lys122Glu
XM_005264326.2:c.364A>G	XP_005264383.1:p.Lys122Glu
XM_005264327.2:c.205A>G	XP_005264384.1:p.Lys69Glu
XM_006712021.2:c.316A>G	XP_006712084.1:p.Lys106Glu
XM_005264326.4:c.364A>G	XP_005264383.1:p.Lys122Glu
XM_006712021.3:c.316A>G	XP_006712084.1:p.Lys106Glu
XM_017004150.1:c.346A>G	XP_016859639.1:p.Lys116Glu
XM_017004151.1:c.316A>G	XP_016859640.1:p.Lys106Glu
XM_017004152.1:c.205A>G	XP_016859641.1:p.Lys69Glu
XM_024452913.1:c.316A>G	XP_024308681.1:p.Lys106Glu
NM_002437.5:c.364A>G MANE Select	NP_002428.1:p.Lys122Glu